293148 <common-name>(1-methylpyrrolidin-3-yl)methyl n-(2-methylphenyl)carbamate</common-name> <description>(1-methylpyrrolidin-3-yl)methyl n-(2-methylphenyl)carbamate belongs to the phenylcarbamic acid esters, a subclass of benzene and substituted derivatives within the organic compounds. This benzenoid compound has the chemical formula C14H20N2O2 and an average molecular weight of 248.32 g/mol.</description> <cas>20930-79-4</cas> <pubchem-id>30367</pubchem-id> <chemical-formula>C14H20N2O2</chemical-formula> <weight>248.32</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">2026-08-28T08:30:14Z</created-at> <updated-at type="dateTime">2026-08-28T08:30:14Z</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>CC1=CC=CC=C1NC(=O)OCC2CCN(C2)C</moldb-smiles> <moldb-formula>C14H20N2O2</moldb-formula> <moldb-inchi>InChI=1S/C14H20N2O2/c1-11-5-3-4-6-13(11)15-14(17)18-10-12-7-8-16(2)9-12/h3-6,12H,7-10H2,1-2H3,(H,15,17)</moldb-inchi> <moldb-inchikey>NYOAGFLQMZLAFC-UHFFFAOYSA-N</moldb-inchikey> <moldb-average-mass type="decimal" nil="true"/> <moldb-mono-mass type="decimal">248.1524779</moldb-mono-mass> <origin nil="true"/> <state nil="true"/> <logp>2.3</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>CHEM289041</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-methylpyrrolidin-3-yl)methyl n-(2-methylphenyl)carbamate</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>Benzene and substituted derivatives</klass> <subklass>Phenylcarbamic acid esters</subklass> <paper-count type="integer" nil="true"/> <sync-id>CED0244679</sync-id> <structure-inchikey>NYOAGFLQMZLAFC-UHFFFAOYSA-N</structure-inchikey> <structure-fingerprint>4000000000000800000000000000010000000000000010000000000000000000000000000000000000004000000000000000000000000000000000000000000000000000000000000000000000020200000000100000000001000000000000000810000000040000000000000000000020100000000000000400004100000000040000000800000000000804080000000000100000080000000000000000040020006000000000000080100000000000000000000008000000000000000000000000000000000000000000000000000008000002000002202000000000000008000000000000040000000000400000000000000000001000000000000</structure-fingerprint> <structure-pattern-fingerprint>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</structure-pattern-fingerprint> <structure-pickle type="binary" encoding="base64">776t3gAAAAAQAAAAAwAAAAAAAAASAAAAEwAAAIABBgBgAAAAAQMGQCgAAAAD BAZAaAAAAAMDAQZAaAAAAAMDAQZAaAAAAAMDAQZAaAAAAAMDAQZAKAAAAAME BwBoAAAAAwIBBgAoAAAAAwQIACgAAAADAggAKAAAAAMCBgBgAAAAAgIGAGAA AAADAQYAYAAAAAICBgBgAAAAAgIHACAAAAADBgBgAAAAAgIGAGAAAAABAwsA AQABAmgMAgNoDAMEaAwEBWgMBQZoDAYHIAcIIAgJKAIICiAKCwALDAAMDQAN DgAODwAPEAAPEQAGAWgMEAwAQgIAAAAGAQYFBAMCBQ0MEA8OFwQAAAAAAAAA Fg== </structure-pickle> <structure-indexed-at type="dateTime">2026-09-19T05:05:07Z</structure-indexed-at> </compound>