497069-39-3

Basic information

• Product Name: 1H-Imidazole-1-carbothioic acid, O-[1-methyl-3-[[(4-methylphenyl)sulfonyl]amino]butyl] ester
• CAS NO: 497069-39-3
• Molecular Formula: C16H21N3O3S2
• Molecular Weight: 367.493
• Mol File: 497069-39-3.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 1H-Imidazole-1-carbothioic acid, O-[1-methyl-3-[[(4-methylphenyl)sulfonyl]amino]butyl] ester(CAS DataBase Reference)
• NIST Chemistry Reference: 1H-Imidazole-1-carbothioic acid, O-[1-methyl-3-[[(4-methylphenyl)sulfonyl]amino]butyl] ester(497069-39-3)
• EPA Substance Registry System: 1H-Imidazole-1-carbothioic acid, O-[1-methyl-3-[[(4-methylphenyl)sulfonyl]amino]butyl] ester(497069-39-3)

Safety Data

• Hazardous Substances Data: 497069-39-3(Hazardous Substances Data)

Upstream product

• 98-59-9 p-toluenesulfonyl chloride 
• 13325-12-7 4-amino-2-pentanol 
• 6160-65-2 1,1'-Thiocarbonyldiimidazole 

Downstream Products

• 2031-38-1 (+/-)-4-methyl-N-(pent-4-en-2-yl)benzenesulfonamide 
• 304460-21-7 rac-4-methyl-N-(pentan-2-yl)benzenesulfonamide 

Relevant articles and documents

Stereoselective radical Aryl migration reactions from sulfur to carbon

Stereoselective aryl migration reactions from sulfur in sulfonates and sulfonamides to C-centered radicals are reported. The 1,5-aryl migration from sulfur to differently substituted C-centered radicals could be performed with high yields and selectivities. Functionalized aryl groups could also be transferred by this new method. A model to explain the stereochemical outcome of the reaction is presented and some mechanistic aspects of this reaction are discussed. Aryl migration reactions from sulfur in sulfinates to carbon radicals were less efficient, and the corresponding migrations in aryl sulfoxides were not observed at all. Wiley-VCH Verlag GmbH, 69451 Weinheim, Germany, 2002.