288589 <common-name>(1,1-dimethyl-3,4-dihydro-2h-quinolin-1-ium-8-yl) n-methylcarbamate</common-name> <description>(1,1-dimethyl-3,4-dihydro-2h-quinolin-1-ium-8-yl) n-methylcarbamate belongs to the hydroquinolines, a subclass of quinolines and derivatives within the organic compounds. It is an organoheterocyclic compound with the formula C13H19N2O2+ and an average molecular weight of 235.30 g/mol.</description> <cas nil="true"/> <pubchem-id>114014</pubchem-id> <chemical-formula>C13H19N2O2+</chemical-formula> <weight>235.3</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">2026-08-28T01:39:55Z</created-at> <updated-at type="dateTime">2026-08-28T01:39:55Z</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>CNC(=O)OC1=CC=CC2=C1[N+](CCC2)(C)C</moldb-smiles> <moldb-formula>C13H19N2O2+</moldb-formula> <moldb-inchi>InChI=1S/C13H18N2O2/c1-14-13(16)17-11-8-4-6-10-7-5-9-15(2,3)12(10)11/h4,6,8H,5,7,9H2,1-3H3/p+1</moldb-inchi> <moldb-inchikey>YDPIWQATJRGNES-UHFFFAOYSA-O</moldb-inchikey> <moldb-average-mass type="decimal" nil="true"/> <moldb-mono-mass type="decimal">235.1446529</moldb-mono-mass> <origin nil="true"/> <state nil="true"/> <logp>1.8</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>CHEM284482</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>(1,1-dimethyl-3,4-dihydro-2h-quinolin-1-ium-8-yl) n-methylcarbamate</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>Organoheterocyclic compounds</superklass> <klass>Quinolines and derivatives</klass> <subklass>Hydroquinolines</subklass> <paper-count type="integer" nil="true"/> <sync-id>CED0240322</sync-id> <structure-inchikey>YDPIWQATJRGNES-UHFFFAOYSA-O</structure-inchikey> <structure-fingerprint>810000000000000000000000000000080000000020000000000000000000000400000000000000000002000000000000000000000000000000008000000000000000000000020000000000102000000000000040000008000010002000000000000000000000100020000000000000000000000000801000040000000800000000000000080000000000000000000080000000000000000000000000000000000080000002000020000000000000000000000000000000000000000010000000000000000000000000008000040204202000000000000000000000000000040004080000400000000000020000000000000000000</structure-fingerprint> <structure-pattern-fingerprint>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</structure-pattern-fingerprint> <structure-pickle type="binary" encoding="base64">776t3gAAAAAQAAAAAwAAAAAAAAARAAAAEgAAAIABBgBgAAAAAQMHAGgAAAAD AgEGACgAAAADBAgAKAAAAAMCCAAoAAAAAwIGQCgAAAADBAZAaAAAAAMDAQZA aAAAAAMDAQZAaAAAAAMDAQZAKAAAAAMEBkAoAAAAAwQHICIAAAABBAYAYAAA AAICBgBgAAAAAgIGAGAAAAACAgYAYAAAAAEDBgBgAAAAAQMLAAEAAQIgAgMo AgIEIAQFIAUGaAwGB2gMBwhoDAgJaAwJCmgMCgsACwwADA0ADQ4ACw8ACxAA CgVoDA4JAEICAAAABgUKCQgHBgYLDA0OCQoXBAAAAAAAAAAW </structure-pickle> <structure-indexed-at type="dateTime">2026-09-19T05:01:46Z</structure-indexed-at> </compound>