214914-14-4

Basic information

• Product Name: 1-(2-allyloxymethyl-phenyl)-1H-imidazole-2-thiol
• CAS NO: 214914-14-4
• Molecular Weight: 246.333
• Mol File: 214914-14-4.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 1-(2-allyloxymethyl-phenyl)-1H-imidazole-2-thiol(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(2-allyloxymethyl-phenyl)-1H-imidazole-2-thiol(214914-14-4)
• EPA Substance Registry System: 1-(2-allyloxymethyl-phenyl)-1H-imidazole-2-thiol(214914-14-4)

Safety Data

• Hazardous Substances Data: 214914-14-4(Hazardous Substances Data)

Upstream product

• 214914-12-2 1-allyloxymethyl-2-isothiocyanato-benzene 
• 214914-31-5 2-(prop-2-enyloxymethyl)benzenamine 
• 214914-13-3 1-(2-allyloxymethyl-phenyl)-3-(2,2-diethoxy-ethyl)-thiourea 

Downstream Products

• 214914-08-6 Acetic acid 2-{2-[(S)-3-(2-oxo-1,2-dihydro-quinolin-6-yloxy)-propane-1-sulfinyl]-imidazol-1-yl}-benzyl ester 
• 214913-88-9 6-{3-[1-(2-hydroxymethyl-phenyl)-1H-imidazole-2-sulfinyl]-propoxy}-3,4-dihydro-1H-quinolin-2-one 
• 214914-09-7 6-{3-[1-(2-hydroxymethyl-phenyl)-1H-imidazole-2-sulfinyl]-propoxy}-1H-quinolin-2-one 
• 214913-85-6 6-{3-[1-(2-hydroxymethyl-phenyl)-1H-imidazol-2-ylsulfanyl]-propoxy}-3,4-dihydro-1H-quinolin-2-one 
• 214913-89-0 6-{3-[1-(2-hydroxymethyl-phenyl)-1H-imidazole-2-sulfinyl]-propoxy}-1H-quinolin-2-one 
• 214913-86-7 6-{3-[1-(2-hydroxymethyl-phenyl)-1H-imidazol-2-ylsulfanyl]-propoxy}-1H-quinolin-2-one 
• 214914-15-5 1-{2-[((E)-Propenyl)oxymethyl]-phenyl}-1H-imidazole-2-thiol 

Relevant articles and documents

An efficient synthesis of optically active metabolites of platelet adhesion inhibitor OPC-29030 by lipase-catalyzed enantioselective transesterification

The optically active metabolites of (S)-3,4-dihydro-6-[3-(1-o-tolyl-2- imidazolyl)sulfinylpropoxy]-2(1H)-quinolinone (OPC-29030, 1), which is a new anti-platelet agent (platelet adhesion inhibitor), were effectively synthesized by the enzyme-catalyzed enantioselective transesterification of the racemic sulfinyl metabolites. The enzymes can recognize a stereogenic sulfur atom remote from the reaction site.