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· · COA & SDS Disponible para cada producto · Same-day shipping on in-stock items P 22077 - ≥98% , CAS No.1247819-59-5
Synonyms
P22077 | HY-13865 | Z1614727651 | 1-[5-(2,4-Difluoro-fenilsulfanil)-4-nitrotiofen-2-il]-etanona | 1-[5-[(2,4-Difluorofenil)tio]-4-nitro-2-tienil]-etanona | FT-0707469 | LGTLXDJOAJDFLR-UHFFFAOYSA- | AC-32695 | SW219709-1 | A899043 | C71981 | EX-A144
Storage
Conservar a -20°C,Desecado
Shipped In
Hielera + almohadillas de hielo
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Why this grade ≥98% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
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Storage & shipping Conservar a -20°C,Desecado 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.
Descripción general Se envía a temperatura ambiente. Almacenar a -20°C. Almacenar en condiciones de desecación.
Specifications Sinónimos
P22077 | HY-13865 | Z1614727651 | 1-[5-(2, 4-Difluoro-fenilsulfanil)-4-nitrotiofen-2-il]-etanona | 1-[5-[(2, 4-Difluorofenil)tio]-4-nitro-2-tienil]-etanona | FT-0707469 | LGTLXDJOAJDFLR-UHFFFAOYSA- | AC-32695 | SW219709-1 | A899043 | C71981 | EX-A144
Especificaciones y pureza
≥98%
Mecanismos bioquímicos y fisiológicos
Inhibidor selectivo de USP7 (IC 50 = 8μM). Activo frente a USP47 estrechamente relacionado. Selectivo frente a SENP2c0re (IC 50 >50\xa0μM) y DENI (IC 50 >50\xa0μM). Desestabiliza Claspin. Inhibe el crecimiento del neuroblastoma induciendo la apoptosis med
Condiciones de almacenamiento de almacenamiento
Conservar a -20°C, Desecado
Enviado en
Hielera + almohadillas de hielo
Nota
Consulte la SDS para obtener más información ¿Necesita más consejos sobre solubilidad, uso y manipulación? Visite nuestra página de preguntas frecuentes (FAQ) para obtener más información.
Nombres e identificadores Pubchem Sid 504770878 Pubchem Sid Url https://pubchem.ncbi.nlm.nih.gov/substance/504770878 Sonrisas canónicas CC(=O)C1=CC(=C(S1)SC2=C(C=C(C=C2)F)F)[N+](=O)[O-] IUPAC Name 1-[5-(2,4-difluorophenyl)sulfanyl-4-nitrothiophen-2-yl]ethanone InChIKey RMAMGGNACJHXHO-UHFFFAOYSA-N INCHI 1S/C12H7F2NO3S2/c1-6(16)11-5-9(15(17)18)12(20-11)19-10-3-2-7(13)4-8(10)14/h2-5H,1H3 Isómeros SMILES CC(=O)C1=CC(=C(S1)SC2=C(C=C(C=C2)F)F)[N+](=O)[O-] PubChem CID 46931953 Número ONU 3077 Grupo de embalaje III Peso molecular 315.32
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 Organosulfur compounds Clase Thioethers Subclass Aryl thioethers Intermediate Tree Nodes Not available Direct Parent Diarylthioethers Alternative Parents 3-nitrothiophenes Thiophenol ethers 2,3,5-trisubstituted thiophenes Aryl alkyl ketones Nitroaromatic compounds Fluorobenzenes Aryl fluorides Heteroaromatic compounds Sulfenyl compounds Propargyl-type 1,3-dipolar organic compounds Organic oxoazanium compounds Organonitrogen compounds Hydrocarbon derivatives Organic oxides Organic salts Organofluorides Organic cations Molecular Framework Aromatic heteromonocyclic compounds Substituents Diarylthioether - 3-nitrothiophene - Nitrothiophene - Nitroaromatic compound - Thiophenol ether - Aryl alkyl ketone - Aryl ketone - 2,3,5-trisubstituted thiophene - Fluorobenzene - Halobenzene - Aryl fluoride - Aryl halide - Monocyclic benzene moiety - Benzenoid - Heteroaromatic compound - Thiophene - Organic nitro compound - Ketone - C-nitro compound - Organic 1,3-dipolar compound - Sulfenyl compound - Allyl-type 1,3-dipolar organic compound - Organoheterocyclic compound - Propargyl-type 1,3-dipolar organic compound - Organic oxoazanium - Organic salt - Organooxygen compound - Organofluoride - Organonitrogen compound - Organohalogen compound - Organic oxygen compound - Organic nitrogen compound - Hydrocarbon derivative - Organic oxide - Organic cation - Aromatic heteromonocyclic compound Descripción This compound belongs to the class of organic compounds known as diarylthioethers. These are organosulfur compounds containing a thioether group that is substituted by two aryl 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 Objetivos asociados (humanos) Objetivos asociados (no humanos) Mecanismos de acción Certificados (CoA, COO, BSE/TSE y tabla de análisis) Propiedades químicas y físicas Solubilidad Soluble in DMSO to 75 mM Peso molecular 315.300 g/mol XLogP3 4.100 Hydrogen Bond Donor Count 0 Hydrogen Bond Acceptor Count 7 Rotatable Bond Count 3 Exact Mass 314.984 Da Monoisotopic Mass 314.984 Da Topological Polar Surface Area 116.000 Ų Heavy Atom Count 20 Formal Charge 0 Complexity 393.000 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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