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· · COA & SDS Disponibile per ogni prodotto · Spedizione lo stesso giorno su articoli in magazzino RN-18 - ≥98% , CAS No.431980-38-0
Synonyms
C75161 | N-(2-methoxyphenyl)-2-((4-nitrophenyl)thio)benzamide | 2-(4-Nitrophenylthio)-N-(2-methoxyphenyl)benzamide | AKOS040742558 | AB00118891-01 | BDBM50534561 | AKOS032953612 | BRD-K43096780-001-01-6 | Oprea1_288287 | [4-[2-[(2-methoxyphenyl)carbamoyl]
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.
Panoramica Information
RN-18 is an inhibitor of HIV-1 viral infectivity factor (HIV-1 Vif) with IC50 of 6 μM in nonpermissive H9 cells.
Specifications Sinonimi
C75161 | N-(2-methoxyphenyl)-2-((4-nitrophenyl)thio)benzamide | 2-(4-Nitrophenylthio)-N-(2-methoxyphenyl)benzamide | AKOS040742558 | AB00118891-01 | BDBM50534561 | AKOS032953612 | BRD-K43096780-001-01-6 | Oprea1_288287 | [4-[2-[(2-methoxyphenyl)carbamoyl]
Meccanismi biochimici e fisiologici
RN-18 is an inhibitor of HIV-1 viral infectivity factor (HIV-1 Vif) with IC50 of 6 μM in nonpermissive H9 cells.
Condizioni di conservazione di stoccaggio
Store at -20°C
Spedito in
Ice chest + Ice pads
Questo prodotto richiede spedizione a catena fredda. I servizi di terra e altri servizi economici non sono disponibili.
Nomi e identificatori Pubchem Sid 528766895 Sorrisi canonici COC1=CC=CC=C1NC(=O)C2=CC=CC=C2SC3=CC=C(C=C3)[N+](=O)[O-] IUPAC Name N-(2-methoxyphenyl)-2-(4-nitrophenyl)sulfanylbenzamide InChIKey JKNUDHUHXMELIJ-UHFFFAOYSA-N INCHI 1S/C20H16N2O4S/c1-26-18-8-4-3-7-17(18)21-20(23)16-6-2-5-9-19(16)27-15-12-10-14(11-13-15)22(24)25/h2-13H,1H3,(H,21,23) Isomeri SMILES COC1=CC=CC=C1NC(=O)C2=CC=CC=C2SC3=CC=C(C=C3)[N+](=O)[O-] PubChem CID 1317590 Peso molecolare 380.42
Documentazione 📋 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 Classe Benzene and substituted derivatives Subclass Anilides Intermediate Tree Nodes Aromatic anilides Direct Parent Benzanilides Alternative Parents Diarylthioethers O-sulfanylbenzoic acids and derivatives Methoxyanilines Nitrobenzenes Benzamides Phenoxy compounds Anisoles Methoxybenzenes Benzoyl derivatives Thiophenol ethers Nitroaromatic compounds Alkyl aryl ethers Vinylogous thioesters Secondary carboxylic acid amides Organic oxoazanium compounds Propargyl-type 1,3-dipolar organic compounds Sulfenyl compounds Hydrocarbon derivatives Organic oxides Organic zwitterions Organonitrogen compounds Organopnictogen compounds Molecular Framework Aromatic homomonocyclic compounds Substituents Benzanilide - Diarylthioether - O-sulfanylbenzoic acid or derivatives - Benzamide - Benzoic acid or derivatives - Nitrobenzene - Methoxyaniline - Nitroaromatic compound - Methoxybenzene - Aryl thioether - Phenoxy compound - Anisole - Benzoyl - Phenol ether - Thiophenol ether - Alkyl aryl ether - Vinylogous thioester - Organic nitro compound - Carboxamide group - C-nitro compound - Secondary carboxylic acid amide - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Allyl-type 1,3-dipolar organic compound - Carboxylic acid derivative - Ether - Organic oxoazanium - Sulfenyl compound - Thioether - Organic nitrogen compound - Hydrocarbon derivative - Organic zwitterion - Organic oxygen compound - Organonitrogen compound - Organooxygen compound - Organosulfur compound - Organopnictogen compound - Organic oxide - Aromatic homomonocyclic compound Descrizione 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.
Struttura 3D Obiettivi associati (umani) Obiettivi associati (non umani) Meccanismi d'azione Certificati (CoA, COO, BSE/TSE e tabella di analisi) Proprietà chimiche e fisiche Peso molecolare 380.400 g/mol XLogP3 4.600 Hydrogen Bond Donor Count 1 Hydrogen Bond Acceptor Count 5 Rotatable Bond Count 5 Exact Mass 380.083 Da Monoisotopic Mass 380.083 Da Topological Polar Surface Area 109.000 Ų Heavy Atom Count 27 Formal Charge 0 Complexity 505.000 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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