Liu, Yu et al. published their research in Proceedings of the National Academy of Sciences of the United States of America in 2014 | CAS: 92557-80-7

2,5-Dioxopyrrolidin-1-yl 3′,6′-dihydroxy-3-oxo-3H-spiro[isobenzofuran-1,9′-xanthene]-5-carboxylate (cas: 92557-80-7) belongs to benzofurans derivatives. Benzofuran is a core structural unit found in many naturally occurring compounds with multidirectional biological activities. Substituted benzofurans find applications such as fluorescent sensors, oxidants, in drug discovery, and in another field of chemistry and agriculture.Application In Synthesis of 2,5-Dioxopyrrolidin-1-yl 3′,6′-dihydroxy-3-oxo-3H-spiro[isobenzofuran-1,9′-xanthene]-5-carboxylate

Small molecule probes to quantify the functional fraction of a specific protein in a cell with minimal folding equilibrium shifts was written by Liu, Yu;Tan, Yun Lei;Zhang, Xin;Bhabha, Gira;Ekiert, Damian C.;Genereux, Joseph C.;Cho, Younhee;Kipnis, Yakov;Bjelic, Sinisa;Baker, David;Kelly, Jeffery W.. And the article was included in Proceedings of the National Academy of Sciences of the United States of America in 2014.Application In Synthesis of 2,5-Dioxopyrrolidin-1-yl 3′,6′-dihydroxy-3-oxo-3H-spiro[isobenzofuran-1,9′-xanthene]-5-carboxylate This article mentions the following:

Although much is known about protein folding in buffers, it remains unclear how the cellular protein homeostasis network functions as a system to partition client proteins between folded and functional, soluble and misfolded, and aggregated conformations. Herein, we develop small mol. folding probes that specifically react with the folded and functional fraction of the protein of interest, enabling fluorescence-based quantification of this fraction in cell lysate at a time point of interest. Importantly, these probes minimally perturb a protein’s folding equilibrium within cells during and after cell lysis, because sufficient cellular chaperone/chaperonin holdase activity is created by rapid ATP depletion during cell lysis. The folding probe strategy and the faithful quantification of a particular protein’s functional fraction are exemplified with retroaldolase, a de novo designed enzyme, and transthyretin, a nonenzyme protein. Our findings challenge the often invoked assumption that the soluble fraction of a client protein is fully folded in the cell. Moreover, our results reveal that the partitioning of destabilized retroaldolase and transthyretin mutants between the aforementioned conformational states is strongly influenced by cytosolic proteostasis network perturbations. Overall, our results suggest that applying a chem. folding probe strategy to other client proteins offers opportunities to reveal how the proteostasis network functions as a system to regulate the folding and function of individual client proteins in vivo. In the experiment, the researchers used many compounds, for example, 2,5-Dioxopyrrolidin-1-yl 3′,6′-dihydroxy-3-oxo-3H-spiro[isobenzofuran-1,9′-xanthene]-5-carboxylate (cas: 92557-80-7Application In Synthesis of 2,5-Dioxopyrrolidin-1-yl 3′,6′-dihydroxy-3-oxo-3H-spiro[isobenzofuran-1,9′-xanthene]-5-carboxylate).

2,5-Dioxopyrrolidin-1-yl 3′,6′-dihydroxy-3-oxo-3H-spiro[isobenzofuran-1,9′-xanthene]-5-carboxylate (cas: 92557-80-7) belongs to benzofurans derivatives. Benzofuran is a core structural unit found in many naturally occurring compounds with multidirectional biological activities. Substituted benzofurans find applications such as fluorescent sensors, oxidants, in drug discovery, and in another field of chemistry and agriculture.Application In Synthesis of 2,5-Dioxopyrrolidin-1-yl 3′,6′-dihydroxy-3-oxo-3H-spiro[isobenzofuran-1,9′-xanthene]-5-carboxylate

Referemce:
Benzofuran – Wikipedia,
Benzofuran | C8H6O – PubChem

Wang, Yuqiang et al. published their research in Journal of Medicinal Chemistry in 2003 | CAS: 89197-62-6

5-Fluorobenzofuran-2-carboxylic acid (cas: 89197-62-6) belongs to benzofurans derivatives. Benzofuran derivatives have shown many biological activities, including antifungal and antimicrobial properties, and acting as antagonists of H3 receptors and angiotensin II. Introduction of benzofurans in organic synthesis, particularly drug synthesis, involves generally the use of their metalated species as nucleophiles in addition reactions or in metal-catalysed cross-coupling reactions.Name: 5-Fluorobenzofuran-2-carboxylic acid

CC-1065 Analogues Bearing Different DNA-Binding Subunits: Synthesis, Antitumor Activity, and Preliminary Toxicity Study was written by Wang, Yuqiang;Li, Lianfa;Ye, Wenqing;Tian, Zhiming;Jiang, Wei;Wang, Hong;Wright, Susan C.;Larrick, James W.. And the article was included in Journal of Medicinal Chemistry in 2003.Name: 5-Fluorobenzofuran-2-carboxylic acid This article mentions the following:

CC-1065 analogs bearing different DNA-binding subunits were synthesized. A terminal C5-NO2 and -F moiety at the DNA-binding subunit increased the drug’s potency and antitumor efficacy. A C5-OCH3 reduced the potency and antitumor efficacy. Compound (±)-I, bearing a trans double bond, had increased antitumor efficacy. A preliminary toxicity study indicated that terminal C5-OCH3 and -acetamido moieties at the DNA-binding subunit caused delayed death in mice. In the experiment, the researchers used many compounds, for example, 5-Fluorobenzofuran-2-carboxylic acid (cas: 89197-62-6Name: 5-Fluorobenzofuran-2-carboxylic acid).

5-Fluorobenzofuran-2-carboxylic acid (cas: 89197-62-6) belongs to benzofurans derivatives. Benzofuran derivatives have shown many biological activities, including antifungal and antimicrobial properties, and acting as antagonists of H3 receptors and angiotensin II. Introduction of benzofurans in organic synthesis, particularly drug synthesis, involves generally the use of their metalated species as nucleophiles in addition reactions or in metal-catalysed cross-coupling reactions.Name: 5-Fluorobenzofuran-2-carboxylic acid

Referemce:
Benzofuran – Wikipedia,
Benzofuran | C8H6O – PubChem

Hu, Yiming et al. published their research in Natural Product Communications in 2022 | CAS: 496-16-2

2,3-Dihydrobenzo[b]furan (cas: 496-16-2) belongs to benzofurans derivatives. Many natural or synthetic compounds containing benzofuran skeletons have been found to possess remarkable activity as agrochemicals and pharmaceuticals. Benzofurans have also made significant and distinctive contributions to biology. They exhibit several biological activities that range from antioxidant, antitubercular, antiplasmodial, insecticidal.Synthetic Route of C8H8O

Dihydrobenzofurans and Propynylthiophenes From the Roots of Eupatorium heterophyllum was written by Hu, Yiming;Saito, Yoshinori;Gong, Xun;Matsuo, Yosuke;Tanaka, Takashi. And the article was included in Natural Product Communications in 2022.Synthetic Route of C8H8O This article mentions the following:

Seven new dihydrobenzofurans and 2 new propynyl thiophenes were isolated from the roots of Eupatorium heterophyllum together with 13 known compounds The compounds were characterized using spectroscopic methods including 2D NMR, IR, and mass spectrometric techniques. Aerial parts of this plant have been known to contain various sesquiterpenoids and displayed high chem. diversity (several compounds isolated and/or identified) among their chem. constituents depending on the collection site. Nevertheless, we found that the chem. diversity in the roots was lower than in the aerial parts. In the experiment, the researchers used many compounds, for example, 2,3-Dihydrobenzo[b]furan (cas: 496-16-2Synthetic Route of C8H8O).

2,3-Dihydrobenzo[b]furan (cas: 496-16-2) belongs to benzofurans derivatives. Many natural or synthetic compounds containing benzofuran skeletons have been found to possess remarkable activity as agrochemicals and pharmaceuticals. Benzofurans have also made significant and distinctive contributions to biology. They exhibit several biological activities that range from antioxidant, antitubercular, antiplasmodial, insecticidal.Synthetic Route of C8H8O

Referemce:
Benzofuran – Wikipedia,
Benzofuran | C8H6O – PubChem

Tannous, Joy H. et al. published their research in Energy & Fuels in 2022 | CAS: 496-16-2

2,3-Dihydrobenzo[b]furan (cas: 496-16-2) belongs to benzofurans derivatives. Benzofurans are only weakly aromatic in nature and they are cleaved by many oxidative and reductive conditions. Introduction of benzofurans in organic synthesis, particularly drug synthesis, involves generally the use of their metalated species as nucleophiles in addition reactions or in metal-catalysed cross-coupling reactions.SDS of cas: 496-16-2

Effect of Solvents on Persistent Free Radical Content in the Absence of Reactions was written by Tannous, Joy H.;Tulegenova, Diana;de Klerk, Arno. And the article was included in Energy & Fuels in 2022.SDS of cas: 496-16-2 This article mentions the following:

The impact of a solvent environment on persistent free radical concentrations at ambient conditions was studied by ESR spectrometry. The analyte selected was Canadian oil-sand-derived bitumen due to its high persistent free radical content. The ability of 54 different solvents to produce a homogeneous 5 wt % solution of bitumen was evaluated. The influence of solvents on the free radical content in bitumen was determined exclusively for solvents that were capable of quant. dissolving the bitumen. These were compounds in the classes of alkynes, mono- and bicyclic benzene-derivatives, and heteroatom-containing compounds containing nitrogen, oxygen, sulfur, and chlorine. It was found that a shift in the g-factor of bitumen occurred when the solvent was changed. The shift was attributed to the radical-solvent interaction that is affected by the polarity of the solvent and reflected in the solvent dipole moment property. The change in the free radical concentration was independent of changes in g-factor and was not correlated with any of the following solvent properties: mol. weight, dipole moment, dielec. constant, refractive index, d., and viscosity. There was a relationship between the free radical concentration in bitumen and the ionization potential of sulfur-containing and diarom. hydrocarbon solvents. It was concluded that the bulk liquid properties that affected the electronic environment of the free radical species, resulting in a shift in g-factor, were not related to the bulk liquid properties that affected the dissociation equilibrium and resulted in a change in the free radical concentration In the experiment, the researchers used many compounds, for example, 2,3-Dihydrobenzo[b]furan (cas: 496-16-2SDS of cas: 496-16-2).

2,3-Dihydrobenzo[b]furan (cas: 496-16-2) belongs to benzofurans derivatives. Benzofurans are only weakly aromatic in nature and they are cleaved by many oxidative and reductive conditions. Introduction of benzofurans in organic synthesis, particularly drug synthesis, involves generally the use of their metalated species as nucleophiles in addition reactions or in metal-catalysed cross-coupling reactions.SDS of cas: 496-16-2

Referemce:
Benzofuran – Wikipedia,
Benzofuran | C8H6O – PubChem

Jayasingha, Jayasingha Arachchige Chathuranga Chanaka et al. published their research in Asian Pacific Journal of Tropical Biomedicine in 2022 | CAS: 1461-15-0

2,2′,2”,2”’-(((3′,6′-Dihydroxy-3-oxo-3H-spiro[isobenzofuran-1,9′-xanthene]-2′,7′-diyl)bis(methylene))bis(azanetriyl))tetraacetic acid (cas: 1461-15-0) belongs to benzofurans derivatives. Benzofuran derivatives are one of the most important oxygen-containing heterocycles. Benzofurans have also made significant and distinctive contributions to biology. They exhibit several biological activities that range from antiviral, antimicrobial, antitumor, anti-inflammatory.Related Products of 1461-15-0

Aqueous extract of freeze-dried Protaetia brevitarsis larvae promotes osteogenesis by activating β-catenin signaling was written by Jayasingha, Jayasingha Arachchige Chathuranga Chanaka;Lee, Kyoung Tae;Choi, Yung Hyun;Kang, Chang-Hee;Lee, Mi-Hwa;Kim, Gi-Young. And the article was included in Asian Pacific Journal of Tropical Biomedicine in 2022.Related Products of 1461-15-0 This article mentions the following:

To investigate the effect of an aqueous extract of Protaetia brevitarsis (AEPB) on osteogenesis using preosteoblast MC3T3-E1 cells and zebrafish larvae. Flow cytometric anal. was used to measure the cytotoxicy. Alk. phosphatase activity was detetmined using p-nitrophenyl phosphate as a substrate. Calcium deposition was detected using alizarin red staining along with osteogenic marker expression in preosteoblast MC3T3E1 cells. In addition, vertebral formation in zebrafish larvae was detected using calcein staining and osteogenic gene expression. AEPB highly promoted the expression of osteogenic markers including runt-related transcription factor 2, osterix, and alk. phosphatase, along with elevated levels of mineralization in MC3T3-E1 cells. Moreover, AEPB accelerated vertebral formation in zebrafish larvae accompanied by upregulated expression of osteogenic genes. FH535, an inhibitor of Wnt/β-catenin, suppressed AEPB-induced osteogenic gene expression and vertebral formation, indicating that AEPB stimulates osteogenesis by activating the Wnt/ β-catenin signaling pathway. AEPB stimulates osteoblast differentiation and bone formation by activating β-catenin. Therefore, AEPB is a promising material that induces osteogenesis, and is useful for the treatment of bone resorption diseases. In the experiment, the researchers used many compounds, for example, 2,2′,2”,2”’-(((3′,6′-Dihydroxy-3-oxo-3H-spiro[isobenzofuran-1,9′-xanthene]-2′,7′-diyl)bis(methylene))bis(azanetriyl))tetraacetic acid (cas: 1461-15-0Related Products of 1461-15-0).

2,2′,2”,2”’-(((3′,6′-Dihydroxy-3-oxo-3H-spiro[isobenzofuran-1,9′-xanthene]-2′,7′-diyl)bis(methylene))bis(azanetriyl))tetraacetic acid (cas: 1461-15-0) belongs to benzofurans derivatives. Benzofuran derivatives are one of the most important oxygen-containing heterocycles. Benzofurans have also made significant and distinctive contributions to biology. They exhibit several biological activities that range from antiviral, antimicrobial, antitumor, anti-inflammatory.Related Products of 1461-15-0

Referemce:
Benzofuran – Wikipedia,
Benzofuran | C8H6O – PubChem

Raditoiu, Valentin et al. published their research in Revista de Chimie (Bucharest, Romania) in 2013 | CAS: 1552-42-7

Crystal violet lactone (cas: 1552-42-7) belongs to benzofurans derivatives. Benzofuran is a core structural unit found in many naturally occurring compounds with multidirectional biological activities. They are also prone to polymerisation in the presence of concentrated mineral acids and Lewis acids.Name: Crystal violet lactone

Thermochromic systems based on complexes of some triarylmethane dyes was written by Raditoiu, Valentin;Raditoiu, Alina;Wagner, Luminita;Amariutei, Viorica;Nicolae, Cristian Andi. And the article was included in Revista de Chimie (Bucharest, Romania) in 2013.Name: Crystal violet lactone This article mentions the following:

The paper presents some triarylmethane dyes and their use in thermochromic systems of donor-accepting type. Compounds are characterized by FT-IR spectra, UV-Vis reflectance spectra and color measurements in CIELAB system and thermal anal. Some considerations are made in relationship with dyestuff structure, developing agent and solvents used to obtain thermochromic systems. The effect of the ratio between the developing agent and lactone dye on the color differences was studied from reflectance spectra and color measurements while the influence of the solvent type on the transition temperature was analyzed using dynamic scanning calorimetry. In the experiment, the researchers used many compounds, for example, Crystal violet lactone (cas: 1552-42-7Name: Crystal violet lactone).

Crystal violet lactone (cas: 1552-42-7) belongs to benzofurans derivatives. Benzofuran is a core structural unit found in many naturally occurring compounds with multidirectional biological activities. They are also prone to polymerisation in the presence of concentrated mineral acids and Lewis acids.Name: Crystal violet lactone

Referemce:
Benzofuran – Wikipedia,
Benzofuran | C8H6O – PubChem

Lopez-Alvarez, Blady et al. published their research in Journal of Hazardous Materials in 2011 | CAS: 1563-38-8

2,2-Dimethyl-2,3-dihydrobenzofuran-7-ol (cas: 1563-38-8) belongs to benzofurans derivatives. Benzofuran is the “”parent”” of many related compounds with more complex structures. For example, psoralen is a benzofuran derivative that occurs in several plants. As benzofurans are prone to undergo ring opening of the heterocycle, examples of reduction of this type of aromatics by using dissolving metals are rather scarce.HPLC of Formula: 1563-38-8

Solar photocatalytical treatment of carbofuran at lab and pilot scale: Effect of classical parameters, evaluation of the toxicity and analysis of organic by-products was written by Lopez-Alvarez, Blady;Torres-Palma, Ricardo A.;Penuela, Gustavo. And the article was included in Journal of Hazardous Materials in 2011.HPLC of Formula: 1563-38-8 This article mentions the following:

The TiO2 solar-photocatalytical degradation of the pesticide carbofuran (CBF) in water, at laboratory- and pilot-scale, was studied. At laboratory-scale the evaluation of CBF concentration (14-282 μmol/L) showed that the system followed a Langmuir-Hinshelwood kinetics type. TiO2 concentration (0.05-2 g/L) and initial pH (3-9) were also evaluated and optimized using the surface response methodol. and the Pareto diagram. In the range of variables studied, initial pH 7.60 and 1.43 g/L of TiO2 favored the efficiency of the process. Under optimal conditions the evolution of substrate, COD, dissolved organic C, toxicity and organics byproducts were evaluated. In the pilot-scale tests, using direct sunlight, 55 mg/L of CBF in a com. formulation was eliminated after 420 min; while after 900 min of treatment 80% of toxicity (1/E50 on Vibrio fischeri), 80% of COD and 60% of dissolved organic C were removed. The anal. and evolution of 5 CBF byproducts, as well the evaluation of the treatment in the presence of isopropanol or using acetonitrile as a solvent suggest that the degradation is mainly carried out by [rad]OH radical attack. A schema depicting the main degradation pathway is proposed. In the experiment, the researchers used many compounds, for example, 2,2-Dimethyl-2,3-dihydrobenzofuran-7-ol (cas: 1563-38-8HPLC of Formula: 1563-38-8).

2,2-Dimethyl-2,3-dihydrobenzofuran-7-ol (cas: 1563-38-8) belongs to benzofurans derivatives. Benzofuran is the “”parent”” of many related compounds with more complex structures. For example, psoralen is a benzofuran derivative that occurs in several plants. As benzofurans are prone to undergo ring opening of the heterocycle, examples of reduction of this type of aromatics by using dissolving metals are rather scarce.HPLC of Formula: 1563-38-8

Referemce:
Benzofuran – Wikipedia,
Benzofuran | C8H6O – PubChem

Shakhtamirov, I. Ya. et al. published their research in Ekologiya Urbanizirovannykh Territorii in 2011 | CAS: 205-39-0

Naphtho[2,1-b]benzofuran (cas: 205-39-0) belongs to benzofurans derivatives. Benzofurans are compounds with a planar structure having 10 pi electrons that include the lone pair on oxygen atom, which makes it more susceptible to electrophilic attack. Benzofurans have also made significant and distinctive contributions to biology. They exhibit several biological activities that range from antioxidant, antitubercular, antiplasmodial, insecticidal.Related Products of 205-39-0

Investigation of air and soil pollution in the residential areas of the city of Grozny by persistent organic pollutants was written by Shakhtamirov, I. Ya.;Amirova, Z. K.. And the article was included in Ekologiya Urbanizirovannykh Territorii in 2011.Related Products of 205-39-0 This article mentions the following:

The results of studies of contamination by persistent organic pollutants (PAHs, PCBs, organochlorine pesticides), air and soil of the city of Grozny. Studies performed in the monitoring of POPs in Europe within the framework of MONET-CEEC regional center for POPs, Brno, Czech Republic. In the experiment, the researchers used many compounds, for example, Naphtho[2,1-b]benzofuran (cas: 205-39-0Related Products of 205-39-0).

Naphtho[2,1-b]benzofuran (cas: 205-39-0) belongs to benzofurans derivatives. Benzofurans are compounds with a planar structure having 10 pi electrons that include the lone pair on oxygen atom, which makes it more susceptible to electrophilic attack. Benzofurans have also made significant and distinctive contributions to biology. They exhibit several biological activities that range from antioxidant, antitubercular, antiplasmodial, insecticidal.Related Products of 205-39-0

Referemce:
Benzofuran – Wikipedia,
Benzofuran | C8H6O – PubChem

Anonymous et al. published their research in Research Disclosure in 1975 | CAS: 13196-10-6

Benzofuran-5-ol (cas: 13196-10-6) belongs to benzofurans derivatives. Benzofuran is a core structural unit found in many naturally occurring compounds with multidirectional biological activities. As benzofurans are prone to undergo ring opening of the heterocycle, examples of reduction of this type of aromatics by using dissolving metals are rather scarce.Electric Literature of C8H6O2

Use of compounds in conjunction with fertilizers was written by Anonymous. And the article was included in Research Disclosure in 1975.Electric Literature of C8H6O2 This article mentions the following:

Compounds of the formula I (where R1 to R4 may be the same or different alkyl groups) are used in conjunction with fast or slow acting fertilizers to retard plant growth. Thus, I (R1 = R2 = R4 = Me; R3 = Et [26225-79-6]) was applied either at the same time or 3-4 weeks subsequent to the application of solid or liquid form fertilizers. When applied as a mixture with a slow-release fertilizer the preferred proportion was 15-60 parts by weight of N and 1-4 parts I. In the experiment, the researchers used many compounds, for example, Benzofuran-5-ol (cas: 13196-10-6Electric Literature of C8H6O2).

Benzofuran-5-ol (cas: 13196-10-6) belongs to benzofurans derivatives. Benzofuran is a core structural unit found in many naturally occurring compounds with multidirectional biological activities. As benzofurans are prone to undergo ring opening of the heterocycle, examples of reduction of this type of aromatics by using dissolving metals are rather scarce.Electric Literature of C8H6O2

Referemce:
Benzofuran – Wikipedia,
Benzofuran | C8H6O – PubChem

Jang, Soo Min et al. published their research in Xenobiotica in 2015 | CAS: 6807-83-6

(2S,3R,4S,5S,6R)-2-(((6aR,12aR)-6a,12a-Dihydro-6H-[1,3]dioxolo[4′,5′:5,6]benzofuro[3,2-c]chromen-3-yl)oxy)-6-(hydroxymethyl)tetrahydro-2H-pyran-3,4,5-triol (cas: 6807-83-6) belongs to benzofurans derivatives. Benzofuran is a core structural unit found in many naturally occurring compounds with multidirectional biological activities. As benzofurans are prone to undergo ring opening of the heterocycle, examples of reduction of this type of aromatics by using dissolving metals are rather scarce.HPLC of Formula: 6807-83-6

Pharmacokinetic properties of trifolirhizin, (-)-maackiain, (-)-sophoranone and 2-(2,4-dihydroxyphenyl)-5,6-methylenedioxybenzofuran after intravenous and oral administration of Sophora tonkinensis extract in rats was written by Jang, Soo Min;Bae, Soo Hyeon;Choi, Woong-Kee;Park, Jung Bae;Kim, Doyun;Min, Jee Sun;Yoo, Hunseung;Kang, Minseok;Ryu, Keun Ho;Bae, Soo Kyung. And the article was included in Xenobiotica in 2015.HPLC of Formula: 6807-83-6 This article mentions the following:

SKI3301, a standardized dried 50% ethanolic extracts of Sophora tonkinensis, contains four marker compounds (trifolirhizin, TF; (-)-maackiain, Maack; (-)-sophoranone, SPN, and (2-(2,4-dihydroxyphenyl)-5,6-methylenedioxybenzofuran, ABF), is being developed as an herbal medicine for the treatment of asthma in Korea. This study investigates the pharmacokinetic properties of SKI3301 extract in rats.2. The dose-proportional AUCs suggest linear pharmacokinetics of TF, Maack, SPN and ABF in the SKI3301 extract i.v. dose range of 5-20 mg/kg. After the oral administration of 200-1000 mg/kg of the extract, TF and Maack exhibited non-linearity due to the saturation of gastrointestinal absorption. However, linear pharmacokinetics of SPN and ABF were observed3. The absorptions of TF, Maack, SPN and ABF in the extract were increased relative to those of the resp. pure forms due to the increased solubility and/or the decreased metabolism by other components in the SKI3301 extract4. No accumulation was observed after multiple dosing, and the steady-state pharmacokinetics of TF, Maack, SPN and ABF were not significantly different from those after a single oral administration of the extract5. The pharmacokinetics of TF, SPN and ABF were not significantly different between male and female rats after oral administration of the extract, but a significant gender difference in the pharmacokinetics of Maack in rats was observed6. Our findings may help to comprehensively elucidate the pharmacokinetic characteristics of TF, Maack, SPN and ABF and provide useful information for the clin. application of SKI3301 extract In the experiment, the researchers used many compounds, for example, (2S,3R,4S,5S,6R)-2-(((6aR,12aR)-6a,12a-Dihydro-6H-[1,3]dioxolo[4′,5′:5,6]benzofuro[3,2-c]chromen-3-yl)oxy)-6-(hydroxymethyl)tetrahydro-2H-pyran-3,4,5-triol (cas: 6807-83-6HPLC of Formula: 6807-83-6).

(2S,3R,4S,5S,6R)-2-(((6aR,12aR)-6a,12a-Dihydro-6H-[1,3]dioxolo[4′,5′:5,6]benzofuro[3,2-c]chromen-3-yl)oxy)-6-(hydroxymethyl)tetrahydro-2H-pyran-3,4,5-triol (cas: 6807-83-6) belongs to benzofurans derivatives. Benzofuran is a core structural unit found in many naturally occurring compounds with multidirectional biological activities. As benzofurans are prone to undergo ring opening of the heterocycle, examples of reduction of this type of aromatics by using dissolving metals are rather scarce.HPLC of Formula: 6807-83-6

Referemce:
Benzofuran – Wikipedia,
Benzofuran | C8H6O – PubChem