Category: 38183-12-9

One-step synthesis of amine-coated ultra-small mesoporous silica nanoparticles was written by Cui, Mingyue;Wiraja, Christian;Qi, Lim Wei;Ting, Sharon Chew Wan;Jana, Deblin;Zheng, Mengjia;Hu, Xiao;Xu, Chenjie. And the article was included in Nano Research in 2020.Formula: C17H10O4 This article mentions the following:

Silica nanoparticles have been studied extensively in biomedical field due to their high biocompatibility, controllable morphol. and so on. They can be used both as the drug carrier and imaging vehicle. Here, an aminated ultra-small silica nanoparticle based system is developed with various functionalities. Multiple mols. including fluorophore, folic acid, and antibody are coupled to this system to achieve specific applications such as bacterial/cell labeling and recognition. [graphic not available: see fulltext]. In the experiment, the researchers used many compounds, for example, 4-Phenyl-3H,3’H-spiro[furan-2,1′-isobenzofuran]-3,3′-dione (cas: 38183-12-9Formula: C17H10O4).

4-Phenyl-3H,3’H-spiro[furan-2,1′-isobenzofuran]-3,3′-dione (cas: 38183-12-9) 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.Formula: C17H10O4

Referemce:
Benzofuran – Wikipedia,
Benzofuran | C8H6O – PubChem

A protective layer approach to solvatochromic sensors was written by Lee, Jung;Chang, Hyun Taek;An, Hyosung;Ahn, Sora;Shim, Jina;Kim, Jong-Man. And the article was included in Nature Communications in 2013.Safety of 4-Phenyl-3H,3’H-spiro[furan-2,1′-isobenzofuran]-3,3′-dione This article mentions the following:

As they have been designed to undergo colorimetric changes that are dependent on the polarity of solvents, the majority of conventional solvatochromic mol. based sensor systems inevitably display broad overlaps in their absorption and emission bands. As a result, colorimetric differentiation of solvents of similar polarity has been extremely difficult. Here we present a tailor-made colorimetric and fluorescence turn-on type solvatochromic sensor that enables facile identification of a specific solvent. The sensor system displays a colorimetric transition only when a thin protective layer, which protects the solvatochromic materials, is destroyed or disrupted by a specific solvent. The versatility of the strategy is demonstrated by designing a sensor that differentiates chloroform and dichloromethane colorimetrically and one that performs sequence selective colorimetric sensing. In addition, the approach is employed to construct a solvatochromic mol. AND logic gate. The new strategy could open new avenues for the development of novel solvatochromic sensors. In the experiment, the researchers used many compounds, for example, 4-Phenyl-3H,3’H-spiro[furan-2,1′-isobenzofuran]-3,3′-dione (cas: 38183-12-9Safety of 4-Phenyl-3H,3’H-spiro[furan-2,1′-isobenzofuran]-3,3′-dione).

4-Phenyl-3H,3’H-spiro[furan-2,1′-isobenzofuran]-3,3′-dione (cas: 38183-12-9) 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. Benzofurans have also made significant and distinctive contributions to biology. They exhibit several biological activities that range from antioxidant, antitubercular, antiplasmodial, insecticidal.Safety of 4-Phenyl-3H,3’H-spiro[furan-2,1′-isobenzofuran]-3,3′-dione

Referemce:
Benzofuran – Wikipedia,
Benzofuran | C8H6O – PubChem

An HPLC method for the determination of moxifloxacin in breast milk by fluorimetric detection with precolumn derivatization was written by Tekkeli, S. E. Kepekci;Gazioglu, I.;Kiziltas, M. V.. And the article was included in Acta Chromatographica in 2017.Name: 4-Phenyl-3H,3’H-spiro[furan-2,1′-isobenzofuran]-3,3′-dione This article mentions the following:

A new, sensitive, and selective high-performance liquid chromatog. (HPLC) method with fluorimetric detection was developed for the determination of moxifloxacin (MOX) in human breast milk. MOX was precolumn derivatized with fluorescamine; the fluorescent derivative was separated on an RP C18 column using a mobile phase composed of acetonitrile-10 mM orthophosphoric acid by isocratic elution with flow rate of 0.5 mL min^-1. The method was based on the measurement of the derivative using fluorescence detection at 481 nm with excitation at 351 nm. The calibration curve was linear over the range of 1-40 μg mL^-1. Limit of detection (LOD) and limit of quantitation (LOQ) were found to be 0.3 and 1 μg mL^-1, resp. Intra-day and interday repeatabilities were less than 3.15%. In the experiment, the researchers used many compounds, for example, 4-Phenyl-3H,3’H-spiro[furan-2,1′-isobenzofuran]-3,3′-dione (cas: 38183-12-9Name: 4-Phenyl-3H,3’H-spiro[furan-2,1′-isobenzofuran]-3,3′-dione).

4-Phenyl-3H,3’H-spiro[furan-2,1′-isobenzofuran]-3,3′-dione (cas: 38183-12-9) belongs to benzofurans derivatives. Benzofuran is a core structural unit found in many naturally occurring compounds with multidirectional biological activities. 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: 4-Phenyl-3H,3’H-spiro[furan-2,1′-isobenzofuran]-3,3′-dione

Referemce:
Benzofuran – Wikipedia,
Benzofuran | C8H6O – PubChem

Improving the in vitro ethoxyresorufin-O-deethylase (EROD) assay with RTL-W1 by metabolic normalization and use of β-naphthoflavone as the reference substance was written by Heinrich, Patrick;Diehl, Ulrike;Foerster, Franziska;Braunbeck, Thomas. And the article was included in Comparative Biochemistry and Physiology, Part C: Toxicology & Pharmacology in 2014.HPLC of Formula: 38183-12-9 This article mentions the following:

The ethoxyresorufin-O-deethylase (EROD) assay is a widely applied method for the evaluation of the dioxin-like activity of single substances and environmental samples. As for most enzyme assays, the specific activity is normally related to total protein contents, the determination of which has clear limitations in high-throughput assays. EROD induction potentials are usually expressed as 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD) equivalent, a substance highly toxic to humans. In order to compensate for these shortcomings, two modifications of the EROD protocol are proposed: (1) EROD activity is normalized to the metabolic activity of the cells as determined by a modified thiazolyl blue tetrazolium (MTT) assay and expressed as metabolic cell equivalent (MCE) based on MTT data rather than to protein contents. Via MCE data, cytotoxicity information can always be reported in parallel to EROD data; with the protocol presented here, MTT and EROD data are collected simultaneously. (2) Among several reference substances tested (2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD), β-naphthoflavone and benzo[a]pyrene), β-naphthoflavone proved to be the most suitable reference for the routine in vitro EROD assay, although TCDD has generally been preferred for purely scientific reasons. In the experiment, the researchers used many compounds, for example, 4-Phenyl-3H,3’H-spiro[furan-2,1′-isobenzofuran]-3,3′-dione (cas: 38183-12-9HPLC of Formula: 38183-12-9).

4-Phenyl-3H,3’H-spiro[furan-2,1′-isobenzofuran]-3,3′-dione (cas: 38183-12-9) belongs to benzofurans derivatives. Many natural or synthetic compounds containing benzofuran skeletons have been found to possess remarkable activity as agrochemicals and pharmaceuticals. 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.HPLC of Formula: 38183-12-9

Referemce:
Benzofuran – Wikipedia,
Benzofuran | C8H6O – PubChem

Microstructural Aspects of Particle-Assisted Breath Figures in Polystyrene-Alumina Hybrid Free Standing Film was written by Vijaya, Lakshmi;Rajan, Ramya;Raju, Annu;Rajan, Thazhavilai Ponnu Devaraj;Pavithran, Chorappan. And the article was included in Journal of Physical Chemistry C in 2017.Recommanded Product: 38183-12-9 This article mentions the following:

Polystyrene-alumina hybrid free standing films with amino-functionalized breath figure (BF) cavities were fabricated from a suspension of the amino-functionalized amphiphilic-modified alumina particles in polystyrene/chloroform solution by employing a one-step casting process. The role of the film thickness and the particle concentration on the BF microstructural aspects such as the pore size, pore d., amino group surface d., etc. was reported. The dry film thickness increased from 0.91 to 5.6 μm on increasing the wet film thickness from 0.2 to 1 mm. The pore size increased with the film thickness, while the pore d. and the porosity decreased. Relatively uniform pore size was observed for an ∼3 μm thick film in which the moderately ordered BF pattern was more or less maintained up to a particle concentration of 5 wt % of the polystyrene content. While the 0.91 μm thick film exhibited through-pore structure, concavities were formed in thicker films. The particle-assisted BF formation favored the formation of amino-functionalized cavities. The surface d. of the amino functionality reduced on increasing the film thickness, whereas the d. increased with the particle concentration The implications were discussed. In the experiment, the researchers used many compounds, for example, 4-Phenyl-3H,3’H-spiro[furan-2,1′-isobenzofuran]-3,3′-dione (cas: 38183-12-9Recommanded Product: 38183-12-9).

4-Phenyl-3H,3’H-spiro[furan-2,1′-isobenzofuran]-3,3′-dione (cas: 38183-12-9) 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. Substituted benzofurans find applications such as fluorescent sensors, oxidants, in drug discovery, and in another field of chemistry and agriculture.Recommanded Product: 38183-12-9

Referemce:
Benzofuran – Wikipedia,
Benzofuran | C8H6O – PubChem

Surface functionalization of silica nanoparticles to enhance aging resistance of asphalt binder was written by Karnati, Sidharth Reddy;Oldham, Daniel;Fini, Elham H.;Zhang, Lifeng. And the article was included in Construction and Building Materials in 2019.HPLC of Formula: 38183-12-9 This article mentions the following:

Oxidation aging of asphalt pavement is among most prevalent factors causing pavement distresses. Introduction of silica nanoparticles (SNPs) has been found promising to reduce oxidation aging of asphalt binder. However, the effectiveness of SNPs is limited by their poor dispersion caused mainly by SNP agglomeration requiring significant mech. energy in processing to ensure dispersion. This paper examined merits of surface functionalization of SNPs with (3-aminopropyl) triethoxysilane (APTES) to improve its dispersion in asphalt binder using conventional processing techniques at relatively high loading of SNPs with low mech. energy input. The morphol., size, amount of amine functional groups of APTES surface-modified SNPs (APTES-SNPs) were characterized and optimized by scanning electron microscope (SEM), dynamic light scattering (DLS), Fourier-transform IR spectroscopy (FTIR) and fluorescence measurement. The comparison between the surface-modified and pristine SNPs on the anti-aging and rheol. properties of asphalt binder was conducted. The asphalt binders which contained APTES-SNPs demonstrated much better resistance to oxidative aging as evidenced by enhanced rheol. properties compared to those containing pristine SNPs. The findings from this research provides insights as to the effect of APTES-SNPs on aging resistance of asphalt binder. In the experiment, the researchers used many compounds, for example, 4-Phenyl-3H,3’H-spiro[furan-2,1′-isobenzofuran]-3,3′-dione (cas: 38183-12-9HPLC of Formula: 38183-12-9).

4-Phenyl-3H,3’H-spiro[furan-2,1′-isobenzofuran]-3,3′-dione (cas: 38183-12-9) 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. 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.HPLC of Formula: 38183-12-9

Referemce:
Benzofuran – Wikipedia,
Benzofuran | C8H6O – PubChem

Aminodextran-coated potassium niobate (KNbO₃) nanocrystals for second harmonic bio-imaging was written by Ladj, Rachid;Magouroux, Thibaud;Eissa, Mohamed;Dubled, Marc;Mugnier, Yannick;Dantec, Ronan Le;Galez, Christine;Valour, Jean-Pierre;Fessi, Hatem;Elaissari, Abdelhamid. And the article was included in Colloids and Surfaces, A: Physicochemical and Engineering Aspects in 2013.Application In Synthesis of 4-Phenyl-3H,3’H-spiro[furan-2,1′-isobenzofuran]-3,3′-dione This article mentions the following:

Potassium niobate (KNbO₃) nanocrystals exhibiting good second harmonic generation properties were coated with dextran derivatives containing primary amine groups. The surface modification results from attractive electrostatic interaction between the aminodextran mols. and the neg. charged surface of bare KNbO₃ nanocrystals. To avoid flocculation, a suspension of KNbO₃ nanocrystals was firstly prepared and then added drop-wise to an aqueous solution of aminodextran. The as-prepared hybrid (AD-coated KNbO₃) nanoparticles were then characterized by using various techniques including transmission electron microscopy (TEM), IR anal. (FTIR), dynamic light scattering (DLS) and zeta potential measurements as a function of pH of the dispersion medium. Then, the prepared AD- coated KNbO₃ nanoparticles were evaluated in vitro diagnostic application as biomarker for non-tumor lung-derived human cells. The obtained results showed that the aminodextran-coated KNbO₃ nanoparticles were efficiently bound to the non-tumor lung-derived human cells, which was proved by using a com. Nikon multi-photon imaging platform. In addition, AD-coated KNbO₃ nanoparticles showed good optical contrast for the investigated cells, and consequently they can be efficiently used as contrast agents in the bio-imaging diagnostic domain. In the experiment, the researchers used many compounds, for example, 4-Phenyl-3H,3’H-spiro[furan-2,1′-isobenzofuran]-3,3′-dione (cas: 38183-12-9Application In Synthesis of 4-Phenyl-3H,3’H-spiro[furan-2,1′-isobenzofuran]-3,3′-dione).

4-Phenyl-3H,3’H-spiro[furan-2,1′-isobenzofuran]-3,3′-dione (cas: 38183-12-9) belongs to benzofurans derivatives. Benzofurans are only weakly aromatic in nature and they are cleaved by many oxidative and reductive conditions. 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.Application In Synthesis of 4-Phenyl-3H,3’H-spiro[furan-2,1′-isobenzofuran]-3,3′-dione

Referemce:
Benzofuran – Wikipedia,
Benzofuran | C8H6O – PubChem

Visualization procedures for proteins and peptides on flat-bed monoliths and their effects on matrix-assisted laser-desorption/ionization time-of-flight mass spectrometric detection was written by Wouters, Bert;Vanhoutte, Dominique J. D.;Aarnoutse, Petra;Visser, Adriaan;Stassen, Catherine;Devreese, Bart;Kok, Wim Th.;Schoenmakers, Peter J.;Eeltink, Sebastiaan. And the article was included in Journal of Chromatography A in 2013.Related Products of 38183-12-9 This article mentions the following:

The present study concerns the application of visualization methods, i.e. coomassie-brilliant-blue-R staining (CBB-R), silver-nitrate staining, and fluorescamine labeling, and subsequent MALDI-MS anal. of intact proteins and peptides on the surface of flat-bed monoliths, intended for spatial two-dimensional chromatog. separations The use of 100-μm thick macroporous poly(Bu methacrylate-co-ethylene dimethacrylate) flat-bed monoliths renders a fixation step obsolete, so that CBB-R and silver-nitrate staining and destaining could be achieved in 10-15 min as opposed to up to 24 h, as is typical on 2D-PAGE gels. The detection limits remained comparable. The compatibility of the monolithic layer with subsequent MALDI-MS anal. of individual proteins and peptide spots was investigated with regards to mass accuracy, mass precision, resolution, and signal intensity. When comparing results from MALDI-MS anal. of proteins and peptides on a flat-bed monolith to results obtained directly on stainless-steel target plates, significant losses in mass precision, signal intensity, and an increased variation in resolution were observed In addition, a loss in signal intensity up to two orders of magnitude was observed when using monolithic layers. After CCB-R and silver-nitrate staining and destaining to disrupt the protein-dye complexes no MALDI spectra with significant S/N ratios could be achieved. After fluorescamine labeling heterogeneous signals were observed, which resulted from a distribution in the number of fluorescence-labeled lysine groups and from the presence of labeled derivatives that had undergone condensation reactions. In the experiment, the researchers used many compounds, for example, 4-Phenyl-3H,3’H-spiro[furan-2,1′-isobenzofuran]-3,3′-dione (cas: 38183-12-9Related Products of 38183-12-9).

4-Phenyl-3H,3’H-spiro[furan-2,1′-isobenzofuran]-3,3′-dione (cas: 38183-12-9) 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. They are also prone to polymerisation in the presence of concentrated mineral acids and Lewis acids.Related Products of 38183-12-9

Referemce:
Benzofuran – Wikipedia,
Benzofuran | C8H6O – PubChem

Covalent cross-links in polyampholytic chitosan fibers enhances bone regeneration in a rabbit model was written by Ghosh, Paulomi;Rameshbabu, Arun Prabhu;Das, Dipankar;Francis, Nimmy K.;Pawar, Harpreet Singh;Subramanian, Bhuvaneshwaran;Pal, Sagar;Dhara, Santanu. And the article was included in Colloids and Surfaces, B: Biointerfaces in 2015.Formula: C17H10O4 This article mentions the following:

Chitosan fibers were prepared in citric acid bath, pH 7.4 and NaOH solution at pH 13, to form ionotropically cross-linked and uncross-linked fibers, resp. The fibers formed in citric acid bath were further cross-linked via carbodiimide chem.; wherein the pendant carboxyl moieties of citric acid were used for new amide bond formation. Moreover, upon covalent crosslinking in the ionically gelled citrate-chitosan fibers, incomplete conversion of the ion pairs to amide linkages took place resulting in the formation of a dual network structure. The dual cross-linked fibers displayed improved mech. property, higher stability against enzymic degradation, hydrophobicity and superior bio-mineralization compared to the uncross-linked and native citrate cross-linked fibers. Addnl., upon cyclic loading, the ion pairs in the dual cross-linked fibers dissociated by dissipating energy and reformed during the relaxation period. The twin property of elasticity and energy dissipation mechanism makes the dual cross-linked fiber unique under dynamic mech. conditions. The differences in the physico-chem. characteristics were reflected in protein adsorption, which in turn influenced the cellular activities on the fibers. Compared to the uncross-linked and ionotropically cross-linked fibers, the dual cross-linked fibers demonstrated higher proliferation and osteogenic differentiation of the MSCs in vitro as well as better osseous tissue regeneration in a rabbit model. In the experiment, the researchers used many compounds, for example, 4-Phenyl-3H,3’H-spiro[furan-2,1′-isobenzofuran]-3,3′-dione (cas: 38183-12-9Formula: C17H10O4).

4-Phenyl-3H,3’H-spiro[furan-2,1′-isobenzofuran]-3,3′-dione (cas: 38183-12-9) belongs to benzofurans derivatives. Benzofuran derivatives are one of the most important oxygen-containing heterocycles. Substituted benzofurans find applications such as fluorescent sensors, oxidants, in drug discovery, and in another field of chemistry and agriculture.Formula: C17H10O4

Referemce:
Benzofuran – Wikipedia,
Benzofuran | C8H6O – PubChem

Gram scale synthesis of Fe/Fe_xO_y core-shell nanoparticles and their incorporation into matrix-free superparamagnetic nanocomposites was written by Watt, John;Bleier, Grant C.;Romero, Zachary W.;Hance, Bradley G.;Bierner, Jessica A.;Monson, Todd C.;Huber, Dale L.. And the article was included in Journal of Materials Research in 2018.Name: 4-Phenyl-3H,3’H-spiro[furan-2,1′-isobenzofuran]-3,3′-dione This article mentions the following:

Significant reductions recently seen in the size of wide-bandgap power electronics have not been accompanied by a relative decrease in the size of the corresponding magnetic components. To achieve this, a new generation of materials with high magnetic saturation and permeability are needed. Here, we develop gram-scale syntheses of superparamagnetic Fe/Fe_xO_y core-shell nanoparticles and incorporate them as the magnetic component in a strongly magnetic nanocomposite. Nanocomposites are typically formed by the organization of nanoparticles within a polymeric matrix. However, this approach can lead to high organic fractions and phase separation; reducing the performance of the resulting material. Here, we form aminated nanoparticles that are then cross-linked using epoxy chem. The result is a magnetic nanoparticle component that is covalently linked and well separated By using this ‘matrix-free’ approach, we can substantially increase the magnetic nanoparticle fraction, while still maintaining good separation, leading to a superparamagnetic nanocomposite with strong magnetic properties. In the experiment, the researchers used many compounds, for example, 4-Phenyl-3H,3’H-spiro[furan-2,1′-isobenzofuran]-3,3′-dione (cas: 38183-12-9Name: 4-Phenyl-3H,3’H-spiro[furan-2,1′-isobenzofuran]-3,3′-dione).

4-Phenyl-3H,3’H-spiro[furan-2,1′-isobenzofuran]-3,3′-dione (cas: 38183-12-9) belongs to benzofurans derivatives. Benzofuran is a core structural unit found in many naturally occurring compounds with multidirectional biological activities. Benzofurans are stable towards alkali and readily polymerize on treatment with sulfuric acid, due to which they are useful for the preparation of low cost chemically relatively inert resins.Name: 4-Phenyl-3H,3’H-spiro[furan-2,1′-isobenzofuran]-3,3′-dione

Referemce:
Benzofuran – Wikipedia,
Benzofuran | C8H6O – PubChem