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· · COA & SDS Disponible para cada producto · Same-day shipping on in-stock items Faisán - ≥98%(HPLC) , CAS No.392721-37-8
Synonyms
SCHEMBL2350751 | STL582160 | BF167835 | GNYIJZMBLZXJEJ-UHFFFAOYSA-N | SR-01000227427-1 | Fasentin | SMSF0013818 | Z57515202 | SR-01000227427 | MFCD01001285 | NCGC00485097-01 | A858091 | HY-101849 | DTXSID60358175 | BS-51102 | CB12214 | AC-36403 | Fasentin
Shipped In
Hielera + almohadillas de hielo
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Why this grade ≥98%(HPLC) for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
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Storage & shipping Conservar a -20°C Ships Hielera + almohadillas de hielo 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 Sinónimos
SCHEMBL2350751 | STL582160 | BF167835 | GNYIJZMBLZXJEJ-UHFFFAOYSA-N | SR-01000227427-1 | Fasentin | SMSF0013818 | Z57515202 | SR-01000227427 | MFCD01001285 | NCGC00485097-01 | A858091 | HY-101849 | DTXSID60358175 | BS-51102 | CB12214 | AC-36403 | Fasentin
Especificaciones y pureza
≥98%(HPLC)
Mecanismos bioquímicos y fisiológicos
Inhibidor de GLUT1 y GLUT4 (IC50= 68 μM). Inhibe preferentemente GLUT4 sobre GLUT1. Sensibiliza al receptor Fas en una serie de líneas celulares tumorales (IC50= 20 μM) modulando la vía apoptótica extrínseca corriente abajo de los receptores TNF pero corr
Condiciones de almacenamiento de almacenamiento
Conservar a -20°C
Enviado en
Hielera + almohadillas de hielo
Nombres e identificadores Sonrisas canónicas CC(=O)CC(=O)NC1=CC(=C(C=C1)Cl)C(F)(F)F IUPAC Name N-[4-chloro-3-(trifluoromethyl)phenyl]-3-oxobutanamide InChIKey GNYIJZMBLZXJEJ-UHFFFAOYSA-N INCHI 1S/C11H9ClF3NO2/c1-6(17)4-10(18)16-7-2-3-9(12)8(5-7)11(13,14)15/h2-3,5H,4H2,1H3,(H,16,18) Isómeros SMILES CC(=O)CC(=O)NC1=CC(=C(C=C1)Cl)C(F)(F)F Peso molecular 279.64 Reaxy-Rn 15650571 Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=15650571&ln=
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 Benzenoids Clase Benzene and substituted derivatives Subclass Trifluoromethylbenzenes Intermediate Tree Nodes Not available Direct Parent Trifluoromethylbenzenes Alternative Parents Anilides N-arylamides Chlorobenzenes Fatty amides Aryl chlorides 1,3-dicarbonyl compounds Secondary carboxylic acid amides Ketones Organopnictogen compounds Organofluorides Organochlorides Organic oxides Hydrocarbon derivatives Alkyl fluorides Molecular Framework Aromatic homomonocyclic compounds Substituents Trifluoromethylbenzene - Anilide - N-arylamide - Chlorobenzene - Halobenzene - Aryl chloride - Aryl halide - Fatty amide - Fatty acyl - 1,3-dicarbonyl compound - Carboxamide group - Secondary carboxylic acid amide - Ketone - Carboxylic acid derivative - Organochloride - Organohalogen compound - Organonitrogen compound - Organooxygen compound - Hydrocarbon derivative - Organic oxide - Alkyl fluoride - Organopnictogen compound - Carbonyl group - Organic oxygen compound - Organic nitrogen compound - Alkyl halide - Organofluoride - Aromatic homomonocyclic compound Descripción This compound belongs to the class of organic compounds known as trifluoromethylbenzenes. These are organofluorine compounds that contain a benzene ring substituted with one or more trifluoromethyl groups. 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.
Estructura 3D Certificados (CoA, COO, BSE/TSE y tabla de análisis) Propiedades químicas y físicas Solubilidad Solvent:DMSO, Max Conc. mg/mL: 27.96, Max Conc. mM: 100; Solvent:ethanol, Max Conc. mg/mL: 27.96, Max Conc. mM: 100 Peso molecular 279.640 g/mol XLogP3 3.700 Hydrogen Bond Donor Count 1 Hydrogen Bond Acceptor Count 5 Rotatable Bond Count 3 Exact Mass 279.027 Da Monoisotopic Mass 279.027 Da Topological Polar Surface Area 46.200 Ų Heavy Atom Count 18 Formal Charge 0 Complexity 333.000 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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