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· · COA & SDS available for every product · Same-day shipping on in-stock items WZB 117 - ≥98% , CAS No.1223397-11-2
Synonyms
EX-A1492 | BCP24665 | BW167833 | [3-fluoro-2-(3-hydroxybenzoyl)oxyphenyl] 3-hydroxybenzoate | AC-32898 | 3-FLUORO-2-(3-HYDROXYBENZOYLOXY)PHENYL 3-HYDROXYBENZOATE | HY-19331 | WZB-117, >=98% (HPLC) | SCHEMBL19183300 | C71842 | s7927 | WZB117 | WZB-117 | 12
Shipped In
Ice chest + Ice pads
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Why this grade ≥98% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
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Storage & shipping Store at -20°C Ships Ice chest + Ice pads Check lot-specific COA for exact specifications.
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Quality documents SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.
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Literature proof Cited in 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
Specifications Synonyms
EX-A1492 | BCP24665 | BW167833 | [3-fluoro-2-(3-hydroxybenzoyl)oxyphenyl] 3-hydroxybenzoate | AC-32898 | 3-FLUORO-2-(3-HYDROXYBENZOYLOXY)PHENYL 3-HYDROXYBENZOATE | HY-19331 | WZB-117, >=98% (HPLC) | SCHEMBL19183300 | C71842 | s7927 | WZB117 | WZB-117 | 12
Specifications & Purity
≥98%
Biochemical and Physiological Mechanisms
GLUT inhibitor (Ki(app)values are 0.2, 10 and 10 μM for GLUT4, GLUT1 and GLUT3, respectively). Competitive inhibitor of net glucose uptake but a noncompetitive inhibitor of sugar efflux from cells. Inhibits passive sugar transport in human erythrocytes an
Shipped In
Ice chest + Ice pads
This product requires cold chain shipping. Ground and other economy services are not available.
Names and Identifiers Pubchem Sid 488201362 Pubchem Sid Url https://pubchem.ncbi.nlm.nih.gov/substance/488201362 Canonical Smiles C1=CC(=CC(=C1)O)C(=O)OC2=C(C(=CC=C2)F)OC(=O)C3=CC(=CC=C3)O IUPAC Name [3-fluoro-2-(3-hydroxybenzoyl)oxyphenyl] 3-hydroxybenzoate InChIKey FRSWCCBXIHFKKY-UHFFFAOYSA-N INCHI 1S/C20H13FO6/c21-16-8-3-9-17(26-19(24)12-4-1-6-14(22)10-12)18(16)27-20(25)13-5-2-7-15(23)11-13/h1-11,22-23H Isomeric SMILES C1=CC(=CC(=C1)O)C(=O)OC2=C(C(=CC=C2)F)OC(=O)C3=CC(=CC=C3)O WGK Germany 3 PubChem CID 46830365 Molecular Weight 368.31
Documentation 📋 Safety Data Sheet (SDS) Comprehensive hazard, handling, storage, and regulatory compliance document.
Download SDS → ✅ Certificate of Analysis (COA) Lot-specific quality data. Enter your lot number to retrieve the exact COA.
Look up COA → 📊 Datasheet Quick-reference summary of product specifications and applications.
View datasheet → 🔬 Specification Sheet Full quality attributes and acceptance criteria for this grade.
View spec sheet →
Advanced Data Taxonomic Classification Kingdom Organic compounds Superclass Phenylpropanoids and polyketides Class Depsides and depsidones Subclass Not available Intermediate Tree Nodes Not available Direct Parent Depsides and depsidones Alternative Parents m-Hydroxybenzoic acid esters Phenol esters Phenoxy compounds Benzoyl derivatives Fluorobenzenes 1-hydroxy-4-unsubstituted benzenoids 1-hydroxy-2-unsubstituted benzenoids Aryl fluorides Carboxylic acid esters Organooxygen compounds Organofluorides Organic oxides Hydrocarbon derivatives Molecular Framework Aromatic homomonocyclic compounds Substituents Depside backbone - M-hydroxybenzoic acid ester - Benzoate ester - Phenol ester - Benzoic acid or derivatives - Phenoxy compound - Benzoyl - 1-hydroxy-4-unsubstituted benzenoid - Fluorobenzene - Halobenzene - 1-hydroxy-2-unsubstituted benzenoid - Phenol - Aryl fluoride - Aryl halide - Monocyclic benzene moiety - Benzenoid - Carboxylic acid ester - Carboxylic acid derivative - Organic oxygen compound - Organohalogen compound - Organofluoride - Organooxygen compound - Hydrocarbon derivative - Organic oxide - Aromatic homomonocyclic compound Description This compound belongs to the class of organic compounds known as depsides and depsidones. These are polycyclic compounds that is either a polyphenolic compound composed of two or more monocyclic aromatic units linked by an ester bond (depside), or a compound containing the depsidone structure (depsidone). External Descriptors Not available Data sources 1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.
3D Structure Associated Targets(Human) Mechanisms of Action Certificates（CoA,COO,BSE/TSE and Analysis Chart) Chemical and Physical Properties Solubility Solvent:DMSO, Max Conc. mg/mL: 36.83, Max Conc. mM: 100; Solvent:ethanol, Max Conc. mg/mL: 36.83, Max Conc. mM: 100 Molecular Weight 368.300 g/mol XLogP3 4.100 Hydrogen Bond Donor Count 2 Hydrogen Bond Acceptor Count 7 Rotatable Bond Count 6 Exact Mass 368.07 Da Monoisotopic Mass 368.07 Da Topological Polar Surface Area 93.100 Ų Heavy Atom Count 27 Formal Charge 0 Complexity 527.000 Isotope Atom Count 0 Defined Atom Stereocenter Count 0 Undefined Atom Stereocenter Count 0 Defined Bond Stereocenter Count 0 Undefined Bond Stereocenter Count 0 The total count of all stereochemical bonds 0 Covalently-Bonded Unit Count 1
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