64768-46-3

Basic information

• Product Name: Benzeneethanesulfonothioic acid, S-(2-phenylethyl) ester
• CAS NO: 64768-46-3
• Molecular Formula: C16H18O2S2
• Molecular Weight: 306.45
• Mol File: 64768-46-3.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: Benzeneethanesulfonothioic acid, S-(2-phenylethyl) ester(CAS DataBase Reference)
• NIST Chemistry Reference: Benzeneethanesulfonothioic acid, S-(2-phenylethyl) ester(64768-46-3)
• EPA Substance Registry System: Benzeneethanesulfonothioic acid, S-(2-phenylethyl) ester(64768-46-3)

Safety Data

• Hazardous Substances Data: 64768-46-3(Hazardous Substances Data)

Upstream product

• 4025-71-2 2-phenylethylsulfonyl chloride 
• 27846-22-6 diphenethyl disulfide 
• 89986-79-8 2-phenetyl sulfinyl chloride 
• 5654-72-8 2-phenylethyl thiocyanate 
• 103-63-9 1-phenyl-2-bromoethane 
• 4410-99-5 2-mercaptophenylethane 

Relevant articles and documents

Direct conversion of sulfinamides to thiosulfonates without the use of additional redox agents under metal-free conditions

Direct conversion of sulfinamides to thiosulfonates is described. Without the use of additional redox agents, the reaction proceeds smoothly in the presence of TFA under metal-free conditions. This protocol possesses many advantages such as odourless and stable starting materials, broad substrate scope, selective synthesis, and mild reaction conditions. This journal is

Tunable and Practical Synthesis of Thiosulfonates and Disulfides from Sulfonyl Chlorides in the Presence of Tetrabutylammonium Iodide

A tunable and practical synthesis of electrophilic sulfenylating reagents, thiosulfonates and disulfides, from inexpensive and easily available sulfonyl chlorides, has been developed. By appropriate choice of solvents, the reaction of sulfonyl chlorides and tetrabutylammonium iodide gave the target products in good to excellent yields, respectively. These transformations probably proceed through a reducing–coupling pathway. (Figure presented.).