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· · COA & SDS available for every product · Same-day shipping on in-stock items 6-chloro-2,3,4,4a,9,9a-hexahydro-1H-carbazole-1-carboxamide , NAD-dependent deacetylase sirtuin 1 inhibitor, CAS No.871586-81-1, NAD-dependent deacetylase sirtuin 1 inhibitor
Synonyms
6-chloro-2,3,4,4a,9,9a-hexahydro-1H-carbazole-1-carboxamide | SCHEMBL18134580 | CHEMBL382277 | BDBM50178783
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Why this grade for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
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Storage & shipping Room temperature Ships 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
6-chloro-2, 3, 4, 4a, 9, 9a-hexahydro-1H-carbazole-1-carboxamide | SCHEMBL18134580 | CHEMBL382277 | BDBM50178783
Mechanism of action
NAD-dependent deacetylase sirtuin 1 inhibitor
Product Properties Names and Identifiers Canonical Smiles C1CC2C(C(C1)C(=O)N)NC3=C2C=C(C=C3)Cl IUPAC Name 6-chloro-2,3,4,4a,9,9a-hexahydro-1H-carbazole-1-carboxamide InChIKey NYORQUCSPQVLTE-UHFFFAOYSA-N INCHI 1S/C13H15ClN2O/c14-7-4-5-11-10(6-7)8-2-1-3-9(13(15)17)12(8)16-11/h4-6,8-9,12,16H,1-3H2,(H2,15,17) Isomeric SMILES C1CC2C(C(C1)C(=O)N)NC3=C2C=C(C=C3)Cl Molecular Weight 250.72 Reaxy-Rn 10261779 Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=10261779&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 Organoheterocyclic compounds Class Indoles and derivatives Subclass Carbazoles Intermediate Tree Nodes Not available Direct Parent Carbazoles Alternative Parents Beta amino acids and derivatives Indolines Secondary alkylarylamines Aralkylamines Benzenoids Aryl chlorides Primary carboxylic acid amides Azacyclic compounds Organochlorides Organic oxides Hydrocarbon derivatives Carbonyl compounds Molecular Framework Aromatic heteropolycyclic compounds Substituents Carbazole - Beta amino acid or derivatives - Dihydroindole - Secondary aliphatic/aromatic amine - Aralkylamine - Aryl chloride - Aryl halide - Benzenoid - Amino acid or derivatives - Carboxamide group - Primary carboxylic acid amide - Carboxylic acid derivative - Azacycle - Secondary amine - Organonitrogen compound - Organochloride - Organohalogen compound - Organic oxide - Carbonyl group - Organic oxygen compound - Organic nitrogen compound - Amine - Organooxygen compound - Hydrocarbon derivative - Aromatic heteropolycyclic compound Description This compound belongs to the class of organic compounds known as carbazoles. These are compounds containing a three ring system containing a pyrrole ring fused on either side to a benzene ring. 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.
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