295760 <common-name>[5-[acetyl(methylsulfonyl)amino]-2-chlorosulfonylnaphthalen-1-yl] acetate</common-name> <description>[5-[acetyl(methylsulfonyl)amino]-2-chlorosulfonylnaphthalen-1-yl] acetate belongs to the naphthalene sulfonic acids and derivatives, a subclass of naphthalenes within the organic compounds. It is a benzenoid with the chemical formula C15H14ClNO7S2 and an average molecular weight of 419.90 g/mol.</description> <cas>71205-36-2</cas> <pubchem-id>117059</pubchem-id> <chemical-formula>C15H14ClNO7S2</chemical-formula> <weight>419.9</weight> <appearance nil="true"/> <melting-point nil="true"/> <boiling-point nil="true"/> <density nil="true"/> <solubility nil="true"/> <specific-gravity nil="true"/> <flash-point nil="true"/> <vapour-pressure nil="true"/> <route-of-exposure nil="true"/> <target nil="true"/> <mechanism-of-toxicity nil="true"/> <metabolism nil="true"/> <toxicity nil="true"/> <lethaldose nil="true"/> <carcinogenicity nil="true"/> <use-source nil="true"/> <min-risk-level nil="true"/> <health-effects nil="true"/> <symptoms nil="true"/> <treatment nil="true"/> <created-at type="dateTime">2026-08-28T11:49:02Z</created-at> <updated-at type="dateTime">2026-08-28T11:49:02Z</updated-at> <interacting-proteins nil="true"/> <wikipedia nil="true"/> <uniprot-id nil="true"/> <kegg-compound-id nil="true"/> <omim-id nil="true"/> <chebi-id nil="true"/> <biocyc-id nil="true"/> <ctd-id nil="true"/> <stitch-id nil="true"/> <drugbank-id nil="true"/> <pdb-id nil="true"/> <actor-id nil="true"/> <organism nil="true"/> <export type="boolean">true</export> <metabolizing-proteins nil="true"/> <transporting-proteins nil="true"/> <moldb-smiles>CC(=O)N(C1=CC=CC2=C1C=CC(=C2OC(=O)C)S(=O)(=O)Cl)S(=O)(=O)C</moldb-smiles> <moldb-formula>C15H14ClNO7S2</moldb-formula> <moldb-inchi>InChI=1S/C15H14ClNO7S2/c1-9(18)17(25(3,20)21)13-6-4-5-12-11(13)7-8-14(26(16,22)23)15(12)24-10(2)19/h4-8H,1-3H3</moldb-inchi> <moldb-inchikey>WHPYMFSZJFUWHZ-UHFFFAOYSA-N</moldb-inchikey> <moldb-average-mass type="decimal" nil="true"/> <moldb-mono-mass type="decimal">418.9900218</moldb-mono-mass> <origin nil="true"/> <state nil="true"/> <logp>1.9</logp> <hmdb-id nil="true"/> <chembl-id nil="true"/> <chemspider-id nil="true"/> <structure-image-file-name nil="true"/> <structure-image-content-type nil="true"/> <structure-image-file-size type="integer" nil="true"/> <structure-image-updated-at type="dateTime" nil="true"/> <biodb-id nil="true"/> <synthesis-reference nil="true"/> <structure-image-caption nil="true"/> <chemdb-id>CHEM291653</chemdb-id> <dsstox-id nil="true"/> <toxcast-id nil="true"/> <stoff-ident-origin nil="true"/> <stoff-ident-id nil="true"/> <susdat-id nil="true"/> <iupac>[5-[acetyl(methylsulfonyl)amino]-2-chlorosulfonylnaphthalen-1-yl] acetate</iupac> <moldb-polar-surface-area nil="true"/> <moldb-refractivity nil="true"/> <moldb-polarizability nil="true"/> <moldb-rotatable-bond-count nil="true"/> <moldb-acceptor-count nil="true"/> <moldb-donor-count nil="true"/> <moldb-pka-strongest-acidic nil="true"/> <moldb-pka-strongest-basic nil="true"/> <moldb-physiological-charge nil="true"/> <moldb-number-of-rings nil="true"/> <moldb-alogps-logp nil="true"/> <moldb-alogps-logs nil="true"/> <moldb-alogps-solubility nil="true"/> <kingdom>Organic compounds</kingdom> <superklass>Benzenoids</superklass> <klass>Naphthalenes</klass> <subklass>Naphthalene sulfonic acids and derivatives</subklass> <paper-count type="integer" nil="true"/> <sync-id>CED0247185</sync-id> <structure-inchikey>WHPYMFSZJFUWHZ-UHFFFAOYSA-N</structure-inchikey> <structure-fingerprint>200000400000000000004000000000000000000000000000000000000000000000000400020000000000800000000000000000000000000000000000000000000000000000000000008020800000000900000000000000000000000000010000000000000000004000004000000000000000000000000000400011000040000000800000000000000000000000000000040000000000000000000000000000000000042000080000000000000000000000080000000000001000000020040108000000000000000000000010000040000045000200000100200000000400000000000040000000000400000000000000000000000020000000</structure-fingerprint> 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