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· · COA & SDS available for every product · Same-day shipping on in-stock items N-(2-chloro-4-nitrophenyl)-1-hydroxynaphthalene-2-carboxamide - ≥97% , CAS No.65570-43-6
Synonyms
MFCD00021479 | SB83327 | SY097943 | AS-50374 | N-(2-Chloro-4-nitrophenyl)-1-hydroxy-2-naphthamide | P10034 | 2'-chloro-1-hydroxy-4'-nitro-2-naphthanilide | SCHEMBL3243499 | C17H11ClN2O4 | N-(2-chloro-4-nitrophenyl)-1-hydroxynaphthalene-2-carboxamide | AKO
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Why this grade ≥97% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
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Storage & shipping Room temperature Ships Normal 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
MFCD00021479 | SB83327 | SY097943 | AS-50374 | N-(2-Chloro-4-nitrophenyl)-1-hydroxy-2-naphthamide | P10034 | 2'-chloro-1-hydroxy-4'-nitro-2-naphthanilide | SCHEMBL3243499 | C17H11ClN2O4 | N-(2-chloro-4-nitrophenyl)-1-hydroxynaphthalene-2-carboxamide | AKO
Specifications & Purity
≥97%
Names and Identifiers Canonical Smiles C1=CC=C2C(=C1)C=CC(=C2O)C(=O)NC3=C(C=C(C=C3)[N+](=O)[O-])Cl IUPAC Name N-(2-chloro-4-nitrophenyl)-1-hydroxynaphthalene-2-carboxamide InChIKey DACDOWVXWKIAAT-UHFFFAOYSA-N INCHI 1S/C17H11ClN2O4/c18-14-9-11(20(23)24)6-8-15(14)19-17(22)13-7-5-10-3-1-2-4-12(10)16(13)21/h1-9,21H,(H,19,22) Isomeric SMILES C1=CC=C2C(=C1)C=CC(=C2O)C(=O)NC3=C(C=C(C=C3)[N+](=O)[O-])Cl Molecular Weight 342.74 Reaxy-Rn 2899336 Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=2899336&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 Class Naphthalenes Subclass Naphthalenecarboxylic acids and derivatives Intermediate Tree Nodes Naphthalenecarboxamides - Naphthalene-2-carboxanilides Direct Parent 1-hydroxynaphthalene-2-carboxanilides Alternative Parents Aromatic anilides Naphthols and derivatives Salicylic acid and derivatives Nitrobenzenes Nitroaromatic compounds 1-hydroxy-4-unsubstituted benzenoids Chlorobenzenes Aryl chlorides Vinylogous acids Secondary carboxylic acid amides Propargyl-type 1,3-dipolar organic compounds Organic oxoazanium compounds Organic oxides Organic salts Hydrocarbon derivatives Organic zwitterions Organochlorides Organonitrogen compounds Organooxygen compounds Molecular Framework Aromatic homopolycyclic compounds Substituents 1-hydroxynaphthalene-2-carboxanilide - Aromatic anilide - 1-naphthol - Salicylic acid or derivatives - Nitrobenzene - Nitroaromatic compound - 1-hydroxy-4-unsubstituted benzenoid - Chlorobenzene - Halobenzene - Phenol - Aryl chloride - Aryl halide - Monocyclic benzene moiety - Vinylogous acid - Organic nitro compound - Carboxamide group - C-nitro compound - Secondary carboxylic acid amide - Organic 1,3-dipolar compound - Carboxylic acid derivative - Propargyl-type 1,3-dipolar organic compound - Allyl-type 1,3-dipolar organic compound - Organic oxoazanium - Organic zwitterion - Organic nitrogen compound - Organic salt - Hydrocarbon derivative - Organic oxide - Organohalogen compound - Organic oxygen compound - Organochloride - Organonitrogen compound - Organooxygen compound - Aromatic homopolycyclic compound Description This compound belongs to the class of organic compounds known as 1-hydroxynaphthalene-2-carboxanilides. These are naphthalene-2-carboxamides, where the carboxamide group is substituted with an aniline, and the naphthalene ring system is hydroxylated at the ring 1-position. 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 Mechanisms of Action Certificates（CoA,COO,BSE/TSE and Analysis Chart) Chemical and Physical Properties Molecular Weight 342.700 g/mol XLogP3 4.700 Hydrogen Bond Donor Count 2 Hydrogen Bond Acceptor Count 4 Rotatable Bond Count 2 Exact Mass 342.041 Da Monoisotopic Mass 342.041 Da Topological Polar Surface Area 95.200 Ų Heavy Atom Count 24 Formal Charge 0 Complexity 484.000 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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