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· · COA & SDS available for every product · Same-day shipping on in-stock items N-(4-Chloro-2,5-dimethoxyphenyl)-3-hydroxy-2-naphthamide - ≥95% , CAS No.4273-92-1
Synonyms
N-(4-chloranyl-2,5-dimethoxy-phenyl)-3-oxidanyl-naphthalene-2-carboxamide | 2-Naphthanilide, 4'-chloro-3-hydroxy-2',5'-dimethoxy- | 4,5,6,7-Tetrachloro-1H-isoindole-1,3(2H)-dione | AS-50333 | MFCD00043903 | SCHEMBL2681368 | BRN 0146082 | cid_77955 | BDBM5
Storage
Room temperature,Desiccated
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Why this grade ≥95% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
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Storage & shipping Room temperature,Desiccated 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
N-(4-chloranyl-2, 5-dimethoxy-phenyl)-3-oxidanyl-naphthalene-2-carboxamide | 2-Naphthanilide, 4'-chloro-3-hydroxy-2', 5'-dimethoxy- | 4, 5, 6, 7-Tetrachloro-1H-isoindole-1, 3(2H)-dione | AS-50333 | MFCD00043903 | SCHEMBL2681368 | BRN 0146082 | cid_77955 | BDBM5
Specifications & Purity
≥95%
Storage
Room temperature, Desiccated
Names and Identifiers Pubchem Sid 488185488 Pubchem Sid Url https://pubchem.ncbi.nlm.nih.gov/substance/488185488 Canonical Smiles COC1=CC(=C(C=C1NC(=O)C2=CC3=CC=CC=C3C=C2O)OC)Cl IUPAC Name N-(4-chloro-2,5-dimethoxyphenyl)-3-hydroxynaphthalene-2-carboxamide InChIKey QIHKTBRNOLQDGQ-UHFFFAOYSA-N INCHI 1S/C19H16ClNO4/c1-24-17-10-15(18(25-2)9-14(17)20)21-19(23)13-7-11-5-3-4-6-12(11)8-16(13)22/h3-10,22H,1-2H3,(H,21,23) Isomeric SMILES COC1=CC(=C(C=C1NC(=O)C2=CC3=CC=CC=C3C=C2O)OC)Cl Molecular Weight 357.79 Reaxy-Rn 3006241 Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=3006241&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 Direct Parent Naphthalene-2-carboxanilides Alternative Parents Aromatic anilides Naphthols and derivatives Salicylic acid and derivatives Dimethoxybenzenes Methoxyanilines Phenoxy compounds Anisoles 1-hydroxy-2-unsubstituted benzenoids Alkyl aryl ethers Chlorobenzenes Aryl chlorides Vinylogous acids Secondary carboxylic acid amides Organic oxides Organochlorides Organonitrogen compounds Organopnictogen compounds Hydrocarbon derivatives Molecular Framework Aromatic homopolycyclic compounds Substituents Naphthalene-2-carboxanilide - Aromatic anilide - 2-naphthol - Salicylic acid or derivatives - Dimethoxybenzene - P-dimethoxybenzene - Methoxyaniline - Anisole - Phenoxy compound - Phenol ether - Methoxybenzene - Alkyl aryl ether - Chlorobenzene - Halobenzene - 1-hydroxy-2-unsubstituted benzenoid - Aryl halide - Monocyclic benzene moiety - Aryl chloride - Vinylogous acid - Secondary carboxylic acid amide - Carboxamide group - Carboxylic acid derivative - Ether - Organic oxide - Organic nitrogen compound - Hydrocarbon derivative - Organochloride - Organonitrogen compound - Organooxygen compound - Organic oxygen compound - Organopnictogen compound - Organohalogen compound - Aromatic homopolycyclic compound Description This compound belongs to the class of organic compounds known as naphthalene-2-carboxanilides. These are naphthalene-2-carboxamides, where the carboxamide group is substituted with an aniline. 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 Associated Targets(Human) Associated Targets(non-human) Mechanisms of Action Certificates（CoA,COO,BSE/TSE and Analysis Chart) Chemical and Physical Properties Flash Point(°C) 244°C Boil Point(°C) 479.8°C at 760 mmHg Melt Point(°C) 190°C Molecular Weight 357.800 g/mol XLogP3 4.800 Hydrogen Bond Donor Count 2 Hydrogen Bond Acceptor Count 4 Rotatable Bond Count 4 Exact Mass 357.077 Da Monoisotopic Mass 357.077 Da Topological Polar Surface Area 67.800 Ų Heavy Atom Count 25 Formal Charge 0 Complexity 463.000 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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