Day: October 17, 2022

Loukhina, I. V.; Gradova, M. A.; Khudyaeva, I. S.; Lobanov, A. V.; Belykh, D. V. published their research in Russian Journal of General Chemistry in 2021. The article was titled 《Synthesis and photocatalytic properties of magnesium silicate modified with cationic chlorin e6 derivatives》.Electric Literature of C20H14O The article contains the following contents:

Synthetic samples of layered magnesium silicate modified with mono-, di-, and tricationic chlorin e6 derivatives have exhibited comparable photochem. activity towards a series of reductants: 1,3-diphenylisobenzofuran selectively oxidizable with singlet oxygen and 1,2-phenylenediamine readily oxidizable with hydrogen peroxide. The optimal photochem. activity of the modified magnesium silicates has been achieved at the ratio of 4-8 μmol of chlorin e6 derivative per 1 g of magnesium silicate. In addition to this study using 1,3-Diphenylisobenzofuran, there are many other studies that have used 1,3-Diphenylisobenzofuran(cas: 5471-63-6Electric Literature of C20H14O) was used in this study.

1,3-Diphenylisobenzofuran(cas: 5471-63-6) can be used as a fluorescent probe for detection of superoxide anion radical (O2−) inside the membrane lipid layer by DPBF fluorescence quenching method. 1,3-Diphenylisobenzofuran(DPBF) can be used to study the single crystal molecular structure and solution photophysical properties of DPBF.Electric Literature of C20H14O

Referemce:
Benzofuran – Wikipedia,
Benzofuran | C8H6O – PubChem

Related Products of 5471-63-6In 2021 ,《Porous polymers from octa(amino-phenyl)silsesquioxane and metalloporphyrin as peroxidase-mimicking enzyme for malathion colorimetric sensor》 appeared in Colloids and Surfaces, B: Biointerfaces. The author of the article were Guo, Xiaojun; Chen, Mohan; Jing, Lu; Li, Jie; Li, Yanhong; Ding, Rui; Zhang, Xiaomei. The article conveys some information:

Rapid and efficient pesticide detection methods are particularly important due to the growing problems of pesticide residues. Here, a new azo-based porous organic polymer, Azo(Fe)PPOP, was prepared from octa(amino-phenyl)silsesquioxane (OAPS) and iron(III) 5,10,15,20-tetrakis(4-nitrophenyl)porphyrin (FeTPP(NO2)4) via a simple coupling reaction without the participation of metal catalysts. The inorganic cage units of OAPS endowed Azo(Fe)PPOP a porous framework, high surface area, favorably thermal and chem. stability. In Azo(Fe)PPOP, iron(III) porphyrin units were individually isolated in a fixed location, which could effectively avoid dimerization or self-oxidation as happens as in the case of porphyrin monomers. Such a unique structure made Azo(Fe)PPOP exhibit an excellent peroxidase-like catalytic performance in the presence of H2O2 and 3,3′,5,5′-tetramethylbenzidine (TMB). Because of these advantages, we established a selective, facile, and sensitive colorimetric platform for direct detection of malathion within a very short time (3 min) with a low detection limit (8.5 nM). In addition, the recognition mechanism between Azo(Fe)PPOP and malathion was verified using XPS spectra. The practicality of the constructed platform was further executed by the detection of the pesticide in soil and food samples. The experimental process involved the reaction of 1,3-Diphenylisobenzofuran(cas: 5471-63-6Related Products of 5471-63-6)

1,3-Diphenylisobenzofuran(cas: 5471-63-6) is a fluorescent dye. 1,3-Diphenylisobenzofuran is the model compound in studies of singlet fission.Related Products of 5471-63-6

Referemce:
Benzofuran – Wikipedia,
Benzofuran | C8H6O – PubChem

Quality Control of 1,3-DiphenylisobenzofuranIn 2021 ,《A Robust Narrow Bandgap Vanadium Tetrasulfide Sonosensitizer Optimized by Charge Separation Engineering for Enhanced Sonodynamic Cancer Therapy》 was published in Advanced Materials (Weinheim, Germany). The article was written by Liang, Shuang; Liu, Bin; Xiao, Xiao; Yuan, Meng; Yang, Ling; Ma, Ping’an; Cheng, Ziyong; Lin, Jun. The article contains the following contents:

The development and optimization of sonosensitizers for elevating intratumoral reactive oxygen species (ROS) are definitely appealing in current sonodynamic therapy (SDT). Given this, branched vanadium tetrasulfide (VS4) nanodendrites with a narrower bandgap (compared with the most extensively explored sonosensitizers) are presented as a new source of sonosensitizer, which allows a more effortless separation of sono-triggered electron-hole pairs for ROS generation. Specifically, platinum (Pt) nanoparticles and endogenous high levels of glutathione (GSH) are rationally engineered to further optimize its sono-sensitized performance. As cocatalyst, Pt is conducive to trapping electrons, whereas GSH, as a natural hole-scavenger, tends to capture holes. Compared with the pristine VS4 sonosensitizer, the GSH-Pt-VS4 nanocomposite can greatly prolong the lifetime of the charge and confer a highly efficacious ROS production activity. Furthermore, such nanoplatforms are capable of reshaping tumor microenvironments to realize ROS overproduction, contributed by overcoming tumor hypoxia to improve SDT-triggered singlet oxygen production, catalyzing endogenic hydrogen peroxide into destructive hydroxyl radicals for chemodynamic therapy, and depleting GSH to amplify intratumoral oxidative stress. All these combined effects result in a significantly efficient tumor suppression outcome. This study enriches sonosensitizer research and proves that sonosensitizers can be rationally optimized by charge separation engineering strategy. In the part of experimental materials, we found many familiar compounds, such as 1,3-Diphenylisobenzofuran(cas: 5471-63-6Quality Control of 1,3-Diphenylisobenzofuran)

1,3-Diphenylisobenzofuran(cas: 5471-63-6) is a fluorescent dye. 1,3-Diphenylisobenzofuran is the model compound in studies of singlet fission.Quality Control of 1,3-Diphenylisobenzofuran

Referemce:
Benzofuran – Wikipedia,
Benzofuran | C8H6O – PubChem

Synthetic Route of C20H14OIn 2021 ,《Conferring Ti-Based MOFs with Defects for Enhanced Sonodynamic Cancer Therapy》 was published in Advanced Materials (Weinheim, Germany). The article was written by Liang, Shuang; Xiao, Xiao; Bai, Lixin; Liu, Bin; Yuan, Meng; Ma, Ping’an; Pang, Maolin; Cheng, Ziyong; Lin, Jun. The article contains the following contents:

The development of highly efficient, multifunctional, and biocompatible sonosensitizer is still a priority for current sonodynamic therapy (SDT). Herein, a defect-rich Ti-based metal-organic framework (MOF) (D-MOF(Ti)) with greatly improved sonosensitizing effect is simply constructed and used for enhanced SDT. Compared with the commonly used sonosensitizer TiO2, D-MOF(Ti) results in a superior reactive oxygen species (ROS) yield under ultrasound (US) irradiation due to its narrow bandgap, which principally improves the US-triggered electron-hole separation Meanwhile, due to the existence of Ti3+ ions, D-MOF(Ti) also exhibits a high level of Fenton-like activity to enable chemodynamic therapy. Particularly, US as the excitation source of SDT can simultaneously enhance the Fenton-like reaction to achieve remarkably synergistic outcomes for oncotherapy. More importantly, D-MOF(Ti) can be degraded and metabolized out of the body after completion of its therapeutic functions without off-target toxicity. Overall, this work identifies a novel Ti-familial sonosensitizer harboring great potential for synergistic sonodynamic and chemodynamic cancer therapy. In the experiment, the researchers used many compounds, for example, 1,3-Diphenylisobenzofuran(cas: 5471-63-6Synthetic Route of C20H14O)

1,3-Diphenylisobenzofuran(cas: 5471-63-6) is a fluorescent dye. 1,3-Diphenylisobenzofuran is the model compound in studies of singlet fission.Synthetic Route of C20H14O

Referemce:
Benzofuran – Wikipedia,
Benzofuran | C8H6O – PubChem

The author of 《Chemistry of the “”insoluble red”” woods. I. Pterocarpin and homopterocarpin》 were McGookin, Alexander; Robertson, Alexander; Whalley, Wm. B.. And the article was published in Journal of the Chemical Society in 1940. Synthetic Route of C12H12O4 The author mentioned the following in the article:

Owing to the insoluble nature of their coloring matters in warm H2O, red sandalwood, camwood, barwood and narrawood have been classified as “”insoluble red”” woods to distinguish them from the “”soluble red”” woods of the logwood type. Since these woods invariably contain the colorless constituents pterocarpin (I) and homopterocarpin (II), they have been studied as an approach to the structure of the dyes. Finely powd. barwood (Baphia nitida Lodd) (300 g.), extracted with 2.5 l. boiling CCl4 for 6 h., the filtered extract concentrated to 37-40 cc. at a temperature not above 50°, 1.5 g. of red solid filtered off, the viscous red liquid dissolved in 20 cc. 96% alc. and the precipitate which seps. fractionally crystallized from 96% EtOH, give 0.15 g. I and 1 g. II, C17H16O4, m. 87°, [α]546120.5 -236.6° (CHCl3, c 0.898 g. in 100 cc.) (cf. Leonhardt and Oechler, C. A. 30, 1372.1). II sublimes unchanged at 80°/0.1 mm. II is extremely sensitive to mineral acids and is stable to boiling EtOH-NaOH; HO or CO groups could not be detected. Oxidation of II with KMnO4 in aqueous Me2CO gives a mixture of 5,2-MeO(HO2C)C6H3OCH2CO2H (IIA) and 2,4-HO(MeO)C6H3CO2H (IIB), indicating the presence of an O-mono-Me resorcinol nucleus and of the system -C.O.CH2C- in II. Catalytic reduction of II in EtOH or AcOH with Pd-C gives l-dihydrohomopterocarpin (III), R = 2,4-HO(MeO)C6H3, m. 154°, [α]546120 -12.7° (EtOH, c 0.295); this is also formed by the Clemmensen reduction of II; the Me ether (IV) m. 61° (cf. Dieterle and L., C. A. 23, 2245). Oxidation of III with CrO3 in AcOH gives dihydrohomopterocarpone (V), orange, m. 177.5-8.5°; oxime, m. 229°. KMnO4 oxidation of III in Me2CO gives 7-methoxy-3-chromancarboxylic acid (VI), m. 149°; the yellow concentrated H2SO4 solution exhibits a brilliant green fluorescence. Reduction of V with Zn and AcOH gives the quinol(?), m. 145°. Oxidation of IV with KMnO4 in Me2CO gives an isoflavanone (VII), R = 2,4-(MeO)2C6H3, m. 127° (oxime, m. 185.5°; 2,4-dinitrophenylhydrazone, red, m. 184°); further oxidation of VII in 2 N NaOH with KMnO4 gives a compound, C15H9O3(OMe)3(?), m. 178°. The 4′-position for the MeO group in III is preferred, although it has not been definitely established. I m. 164.5° [α]546120.5 -207.5° (CHCl3, c 0.530). Hydrogenation of I in AcOH with Pd-C gives a dihydro derivative (VIII), m. 140°, [α]546121 -19.5° (EtOH, c 1.714), which also results on Clemmensen reduction of I; Me ether (IX), m. 106.5°. Oxidation of I with KMnO4 in aqueous Me2CO gives a mixture of IIA and IIB, with a small amount of a neutral product, m. 272°. VIII gives VI with KMnO4 in aqueous Me2CO and with CrO8 in AcOH there results a yellow resinous product which with 2,4-(O2N)2C6H3NHNH2 gives a compound, C23H18O10N4, maroon, m. 202-3° (decomposition). KMnO4 oxidation of IX yields a ketone, C16H10O4(OMe)2, m. 118-19°, whose 2,4-dinitrophenylhydrazone, scarlet, m. 248°. Thus, I appears to differ from II in having a methylenedioxy group. 4-O-Methyl-β-resorcylaldehyde in 8% aqueous KOH, added to ClCH2CH2CO2H in aqueous NaHCO3, gives β-(5-methoxy-2-formylphenoxy)propionic acid, m. 159°; 2,4-dinitrophenylhydrazone, m. 241.5°; semicarbazone, m. 218° (decomposition); oxidation with alk. KMnO4 gives β-(5-methoxy-2-carboxyphenoxy)propionic acid, m. 143°; Me ester, b95 78-80°. The acid, Ac2O and AcONa, refluxed 1 h. at 145°, give 7-methoxy-Δ3-chromene-3-carboxylic acid, m. 201°; the yellow concentrated H2SO4 has an intense green fluorescence; catalytic reduction gives VI. 2,5-OHC(MeO)C6H3OCH2CO2Et gives a 2,4-dinitrophenylhydrazone, crimson, m. 176.5°; cyclization of the ester with EtONa in EtOH gives Et 6-methoxy-2-coumaronecarboxylate (X), m. 87°; it gives a cherry-red and then a purple H2SO4 reaction; acidification of the alk. liquor gives 2,5-OHC(MeO)C6H3OCH2CO2H, yielding a 2,4-dinitrophenylhydrazone, light red, m. 273°. The free acid from X m. 206°, having a crimson and then a brilliant purple H2SO4 reaction; PCl5 in CHCl3 gives the acid chloride (XI), b15 165°, m. 101°. XI in absolute ether at -10° with anhydrous HCN and a mixture of C5H5N and ether gives the nitrile, pale yellow, b1.5 162°, m. 101°; this could not be converted into the corresponding pyruvic acid. XI and CH2N2 in ether give the diazoketone, pale yellow, m. 90-1° (slight decomposition); with NH4OH and AgNO3 in dioxane there results the amide, m. 148°, of 6-methoxy-2-coumaroneacetic acid, m. 104°. In addition to this study using Ethyl 6-methoxybenzofuran-2-carboxylate, there are many other studies that have used Ethyl 6-methoxybenzofuran-2-carboxylate(cas: 50551-57-0Synthetic Route of C12H12O4) was used in this study.

Ethyl 6-methoxybenzofuran-2-carboxylate(cas: 50551-57-0) belongs to benzofurans.Synthetic Route of C12H12O4Benzofurans containing one furan ring that have been implicated as psychoactive recreational drugs include 6-(2-aminopropyl)benzofuran (6-APB), 5-(2-aminopropyl)benzofuran (5-APB), 5-(2-ethylaminopropyl)benzofuran (5-EAPB), and 5-methylaminopropylbenzofuran (5-MAPB).

Referemce:
Benzofuran – Wikipedia,
Benzofuran | C8H6O – PubChem

《Photophysical and electrochemical properties of two trans-A2B-corroles: differences between phenyl or pyrenyl groups at the meso-10 position》 was written by Acunha, Thiago V.; Victoria, Henrique F. V.; Krambrock, Klaus; Marques, Amanda C.; Costa, Luiz Antonio S.; Iglesias, Bernardo A.. Quality Control of 1,3-Diphenylisobenzofuran And the article was included in Physical Chemistry Chemical Physics in 2020. The article conveys some information:

The present study reported on the optical and photophys. properties of trans-A2B-corroles possessing pyrenyl units attached at the meso-10-position and compares them with those of model trans-A2B-corroles having Ph substituents at that position. In contrast to the model meso-substituted corrole, the new pyrenyl-corrole showed slightly red-shifted absorption bands and blue-shifted emission, slightly higher fluorescence quantum yield, and more importantly, it showed better photo-stability under white-light illumination. Theor. calculations were used to determine the electronic transitions and geometries of the singlet and triplet excited states (TD-DFT and NTO). Moreover, we demonstrated that the pyrenyl-corrole in analogy to previously studied model corroles was able to generate reactive oxygen species (ROS) under visible light using photo-degradation of 1,3-diphenylisobenzofuran (DBPF), a singlet oxygen quencher, and EPR spectroscopy allied with the spin-trapping method was used for identifying singlet oxygen species. The results showed that the pyrenyl unit attached at the meso-10-position of the corrole increased the photo-stability and efficiency in ROS generation compared to the Ph substituent.1,3-Diphenylisobenzofuran(cas: 5471-63-6Quality Control of 1,3-Diphenylisobenzofuran) was used in this study.

1,3-Diphenylisobenzofuran(cas: 5471-63-6) can be used as a fluorescent probe for detection of superoxide anion radical (O2−) inside the membrane lipid layer by DPBF fluorescence quenching method. 1,3-Diphenylisobenzofuran(DPBF) can be used as quencher during the photoinactivation of TA-3 mouse mammary carcinoma cells containing hematoporphyrin.Quality Control of 1,3-Diphenylisobenzofuran

Referemce:
Benzofuran – Wikipedia,
Benzofuran | C8H6O – PubChem

《Generation and Reactivity of a NiIII2(μ-1,2-peroxo) Complex》 was written by Zhao, Norman; Filatov, Alexander S.; Xie, Jiaze; Hill, Ethan A.; Rogachev, Andrey Yu.; Anderson, John S.. HPLC of Formula: 5471-63-6 And the article was included in Journal of the American Chemical Society in 2020. The article conveys some information:

High-valent transition metal-oxo, -peroxo, and -superoxo complexes are crucial intermediates in both biol. and synthetic oxidation of organic substrates, water oxidation, and oxygen reduction While high-valent oxygenated complexes of Mn, Fe, Co, and Cu are increasingly known, high-valent oxygenated Ni complexes are comparatively rarer. Herein authors report the isolation of such an unusual high-valent species in a thermally unstable NiIII2(μ-1,2-peroxo) complex, which was characterized using single-crystal x-ray diffraction and x-ray absorption, NMR, and UV-visible spectroscopies. Reactivity studies show that this complex is stable toward dissociation of oxygen but reacts with simple nucleophiles and electrophiles.1,3-Diphenylisobenzofuran(cas: 5471-63-6HPLC of Formula: 5471-63-6) was used in this study.

1,3-Diphenylisobenzofuran(cas: 5471-63-6) can be used as a fluorescent probe for detection of superoxide anion radical (O2−) inside the membrane lipid layer by DPBF fluorescence quenching method. 1,3-Diphenylisobenzofuran(DPBF) can be used as quencher during the photoinactivation of TA-3 mouse mammary carcinoma cells containing hematoporphyrin.HPLC of Formula: 5471-63-6

Referemce:
Benzofuran – Wikipedia,
Benzofuran | C8H6O – PubChem

Romero, Maria P; Buzza, Hilde H; Stringasci, Mirian D; Estevão, Bianca M; Silva, Cecilia C C; Pereira-da-Silva, Marcelo A; Inada, Natalia M; Bagnato, Vanderlei S published their research in International journal of nanomedicine in 2021. The article was titled 《Graphene Oxide Theranostic Effect: Conjugation of Photothermal and Photodynamic Therapies Based on an in vivo Demonstration.》.Application of 5471-63-6 The article contains the following contents:

INTRODUCTION: Cancer is the second leading cause of death globally and is responsible, where about 1 in 6 deaths in the world. Therefore, there is a need to develop effective antitumor agents that are targeted only to the specific site of the tumor to improve the efficiency of cancer diagnosis and treatment and, consequently, limit the unwanted systemic side effects currently obtained by the use of chemotherapeutic agents. In this context, due to its unique physical and chemical properties of graphene oxide (GO), it has attracted interest in biomedicine for cancer therapy. METHODS: In this study, we report the in vivo application of nanocomposites based on Graphene Oxide (nc-GO) with surface modified with PEG-folic acid, Rhodamine B and Indocyanine Green. In addition to displaying red fluorescence spectra Rhodamine B as the fluorescent label), in vivo experiments were performed using nc-GO to apply Photodynamic Therapy (PDT) and Photothermal Therapy (PTT) in the treatment of Ehrlich tumors in mice using NIR light (808 nm 1.8 W/cm2). RESULTS: This study based on fluorescence images was performed in the tumor in order to obtain the highest concentration of nc-GO in the tumor as a function of time (time after intraperitoneal injection). The time obtained was used for the efficient treatment of the tumor by PDT/PTT. DISCUSSION: The current study shows an example of successful using nc-GO nanocomposites as a theranostic nanomedicine to perform simultaneously in vivo fluorescence diagnostic as well as combined PDT-PTT effects for cancer treatments. The results came from multiple reactions, including the reaction of 1,3-Diphenylisobenzofuran(cas: 5471-63-6Application of 5471-63-6)

1,3-Diphenylisobenzofuran(cas: 5471-63-6) can be used as a fluorescent probe for detection of superoxide anion radical (O2−) inside the membrane lipid layer by DPBF fluorescence quenching method. 1,3-Diphenylisobenzofuran(DPBF) can be used to study the single crystal molecular structure and solution photophysical properties of DPBF.Application of 5471-63-6

Referemce:
Benzofuran – Wikipedia,
Benzofuran | C8H6O – PubChem

In 2022,Wang, Ya-Ning; Zhang, Wen-Shu; Liu, Xiao-Peng; Wei, Yun-Yun; Xu, Zhang-Run published an article in Colloids and Surfaces, B: Biointerfaces. The title of the article was 《A nanohybrid of Prussian blue supported by boracic acid-modified g-C3N4 for Raman recognition of cell surface sialic acid and photothermal/photodynamic therapy》.SDS of cas: 5471-63-6 The author mentioned the following in the article:

Theranostic nanoplatforms with accurate diagnosis and effective therapy show a bright prospect for tumor treatments. Herein, a novel boracic acid-modified graphite carbon nitride and Prussian blue nanohybrid (PB@B-g-3N4) was developed, which provides sialic acid-targeted Raman recognition and synergistic photothermal/photodynamic therapy in the near-IR region. Owing to the specific interaction between boracic acid and sialic acid and Raman response at 2157 cm-1 of PB, the nanohybrids exhibit high specificity and Raman sensitivity for detection of the overexpressed sialic acid on tumor cells. Moreover, the photothermal conversion efficiency of PB@B-g-3N4 is as high as 47.0% with 808 nm laser irradiation due to the enhanced absorbance of PB@B-g-3N4. PB@B-g-3N4 also possesses excellent photodynamic activity, which is attributed to the energy transfer of PB (type I) and electron transfer between PB and B-g-3N4 (type II). This nanotheranostic agent for Raman recognition of cancer markers and synergistic photothermal/photodynamic therapy holds great potential for the development of efficient theranostic nanoplatforms. The experimental part of the paper was very detailed, including the reaction process of 1,3-Diphenylisobenzofuran(cas: 5471-63-6SDS of cas: 5471-63-6)

1,3-Diphenylisobenzofuran(cas: 5471-63-6) can be used as a fluorescent probe for detection of superoxide anion radical (O2−) inside the membrane lipid layer by DPBF fluorescence quenching method. 1,3-Diphenylisobenzofuran(DPBF) can be used as quencher during the photoinactivation of TA-3 mouse mammary carcinoma cells containing hematoporphyrin.SDS of cas: 5471-63-6

Referemce:
Benzofuran – Wikipedia,
Benzofuran | C8H6O – PubChem

《A bacteria-triggered wearable colorimetric band-aid for real-time monitoring and treating of wound healing》 was written by Dong, Mengna; Sun, Xinyu; Li, Lihua; He, Kunyi; Wang, Jiao; Zhang, Hui; Wang, Li. Computed Properties of C20H14OThis research focused onwearable colorimetric band aid wound healing bacterial infection; Film-based band-aid; PDT/PTT; Wearable; Wound healing; pH-sensing. The article conveys some information:

Early diagnosis of bacterial infection and tracking of treatment effect are of great importance for developing a “”sense-and-treat”” integrated system. Herein, we developed a bacteria-triggered, portable, wearable and colorimetric film-based band-aid (FBA) for closed-loop monitoring and light-controlled therapy of wound infection. FBA with high photothermal conversion efficiency of 52.56% was prepared by wrapping Bi2S3 nanoflowers (BS NFs) loaded with rhodium nanoparticles (Rh NPs) and bromothymol blue (BTB) into LB agar film, integrating bacteria-triggered color change, photothermal/photodynamic therapy (PTT/PDT) synergistic bactericidal therapy and agar-based band aid in one intelligent system. Initially, FBA effectively simulates the pH sensing mechanism, and monitors the occurrence of bacterial infections within 5 min through color changes of Staphylococcus aureus (S. aureus) from blue to yellow and Escherichia coli (E. coli) from yellow to blue. Addnl., the short-term and controlled antibacterial strategy of “”one light dual-mode responses”” (photothermal and photodynamic responses) was implemented with the introduce of near-IR (NIR). Ultimately, the effectiveness of FBA was fully validated in the monitoring and treating of S. aureus-infected mouse wounds. Notably, the designed FBA decisively abandoned off-target side effects maximizing the treatment effect and nakedly tracking therapeutic situation in real time, contributing an effective antibacterial alternative strategy for reducing the use of antibiotics. To the best of our knowledge, such integrated system is still unreported on film-fixed model. In view of the advantages of the low cost and convenience of the simple device, the integrated design is expected to provide a solution for the development of a closed-loop biomedical system combining diagnosis and treatment. In the experimental materials used by the author, we found 1,3-Diphenylisobenzofuran(cas: 5471-63-6Computed Properties of C20H14O)

1,3-Diphenylisobenzofuran(cas: 5471-63-6) is a fluorescent dye. 1,3-Diphenylisobenzofuran is the model compound in studies of singlet fission.Computed Properties of C20H14O

Referemce:
Benzofuran – Wikipedia,
Benzofuran | C8H6O – PubChem