CHEBI:8102 - phenylmethanesulfonyl fluoride

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ChEBI Name phenylmethanesulfonyl fluoride ChEBI ID CHEBI:8102 Definition An acyl fluoride with phenylmethanesulfonyl as the acyl group. Stars This entity has been manually annotated by the ChEBI Team. Supplier Information Download Molfile XML SDF Find compounds which contain this structure Find compounds which resemble this structure Take structure to the Advanced Search Wikipedia License Read full article at Wikipedia Formula C7H7FO2S Net Charge 0 Average Mass 174.19368 Monoisotopic Mass 174.01508 InChI InChI=1S/C7H7FO2S/c8-11(9,10)6-7-4-2-1-3-5-7/h1-5H,6H2 InChIKey YBYRMVIVWMBXKQ-UHFFFAOYSA-N SMILES FS(=O)(=O)Cc1ccccc1 Roles Classification Biological Role(s): serine proteinase inhibitor An exogenous or endogenous compound which inhibits serine endopeptidases. View more via ChEBI Ontology ChEBI Ontology Outgoing phenylmethanesulfonyl fluoride (CHEBI:8102) has functional parent phenylmethanesulfonic acid (CHEBI:38112) phenylmethanesulfonyl fluoride (CHEBI:8102) has role serine proteinase inhibitor (CHEBI:48353) phenylmethanesulfonyl fluoride (CHEBI:8102) is a acyl fluoride (CHEBI:38110) IUPAC Name phenylmethanesulfonyl fluoride Synonyms Sources α-toluenesulfonyl fluoride ChemIDplus α-toluenesulphonyl fluoride ChemIDplus Benzenemethanesulfonyl fluoride KEGG COMPOUND Phenylmethanesulfonyl fluoride KEGG COMPOUND phenylmethylsulfonyl fluoride ChemIDplus PMSF KEGG COMPOUND Manual Xrefs Databases C06747 KEGG COMPOUND CPD-5541 MetaCyc LSM-37050 LINCS Phenylmethanesulfonylfluoride Wikipedia View more database links Registry Numbers Types Sources 2088311 Beilstein Registry Number ChemIDplus 2088311 Reaxys Registry Number Reaxys 329-98-6 CAS Registry Number ChemIDplus Citations Types Sources 23290539 PubMed citation Europe PMC 24211707 PubMed citation Europe PMC Last Modified 26 February 2016