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· · COA & SDS Disponible para cada producto · Same-day shipping on in-stock items 4-Bromo-N-(4-bromophenyl)-3-[[(phenylmethyl)amino]sulfonyl]benzamide - 10mM in DMSO , CAS No.312756-74-4
GRADE & PURITY 10mM in DMSO
Synonyms
3-[(benzylamino)sulfonyl]-4-bromo-N-(4-bromophenyl)benzamide | AC-35367 | 3-(N-Benzylsulfamoyl)-4-bromo-N-(4-bromophenyl)benzamide | HY-19793 | 3-(benzylsulfamoyl)-4-bromo-N-(4-bromophenyl)benzamide | J46 | Oprea1_166111 | EU-0034229 | Benzamide, 4-bromo-
Shipped In
Dry ice packs + Cold packs
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Why this grade 10mM in DMSO for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
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Storage & shipping Store at -80°C Ships Dry ice packs + Cold packs 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
3-[(benzylamino)sulfonyl]-4-bromo-N-(4-bromophenyl)benzamide | AC-35367 | 3-(N-Benzylsulfamoyl)-4-bromo-N-(4-bromophenyl)benzamide | HY-19793 | 3-(benzylsulfamoyl)-4-bromo-N-(4-bromophenyl)benzamide | J46 | Oprea1_166111 | EU-0034229 | Benzamide, 4-bromo-
Especificaciones y pureza
10mM in DMSO
Mecanismos bioquímicos y fisiológicos
RAD51-Stimulatory Compound-1, RS-1 is a cell-permeable sulfonamido-benzamide compound which acts as an allosteric effector of active human RAD51 filament structure and stimulates DNA binding and recombination activities of hRAD51 protein. RS-1 is shown to
Condiciones de almacenamiento de almacenamiento
Store at -80°C
Enviado en
Dry ice packs + Cold packs
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Nombres e identificadores Sonrisas canónicas C1=CC=C(C=C1)CNS(=O)(=O)C2=C(C=CC(=C2)C(=O)NC3=CC=C(C=C3)Br)Br IUPAC Name 3-(benzylsulfamoyl)-4-bromo-N-(4-bromophenyl)benzamide InChIKey SWKAVEUTKGKHSR-UHFFFAOYSA-N INCHI 1S/C20H16Br2N2O3S/c21-16-7-9-17(10-8-16)24-20(25)15-6-11-18(22)19(12-15)28(26,27)23-13-14-4-2-1-3-5-14/h1-12,23H,13H2,(H,24,25) Isómeros SMILES C1=CC=C(C=C1)CNS(=O)(=O)C2=C(C=CC(=C2)C(=O)NC3=CC=C(C=C3)Br)Br WGK Alemania 3 Peso molecular 524.23 Reaxy-Rn 26855890 Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=26855890&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 Anilides Intermediate Tree Nodes Aromatic anilides Direct Parent Benzanilides Alternative Parents 4-halobenzoic acids and derivatives Benzenesulfonamides Benzamides Benzenesulfonyl compounds Benzoyl derivatives Bromobenzenes Organosulfonamides Aryl bromides Aminosulfonyl compounds Secondary carboxylic acid amides Hydrocarbon derivatives Organic oxides Organobromides Organonitrogen compounds Organooxygen compounds Organopnictogen compounds Molecular Framework Aromatic homomonocyclic compounds Substituents Benzanilide - Benzenesulfonamide - 4-halobenzoic acid or derivatives - Halobenzoic acid or derivatives - Benzamide - Benzoic acid or derivatives - Benzenesulfonyl group - Benzoyl - Bromobenzene - Halobenzene - Organosulfonic acid amide - Aryl halide - Aryl bromide - Sulfonyl - Organosulfonic acid or derivatives - Organic sulfonic acid or derivatives - Aminosulfonyl compound - Secondary carboxylic acid amide - Carboxamide group - Carboxylic acid derivative - Organosulfur compound - Organohalogen compound - Organobromide - Organonitrogen compound - Organic oxide - Organopnictogen compound - Organic oxygen compound - Organic nitrogen compound - Organooxygen compound - Hydrocarbon derivative - Aromatic homomonocyclic compound Descripción This compound belongs to the class of organic compounds known as benzanilides. These are aromatic compounds containing an anilide group in which the carboxamide group is substituted with a benzene ring. They have the general structure RNC(=O)R', where R,R'= benzene. 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 Sensibilidad Air Sensitive,Moisture Sensitive,Heat Sensitive Punto de fusión (°C) 208 °C Peso molecular 524.200 g/mol XLogP3 4.600 Hydrogen Bond Donor Count 2 Hydrogen Bond Acceptor Count 4 Rotatable Bond Count 6 Exact Mass 523.923 Da Monoisotopic Mass 521.925 Da Topological Polar Surface Area 83.700 Ų Heavy Atom Count 28 Formal Charge 0 Complexity 611.000 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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