107033-47-6

Basic information

• Product Name: (2R,3R)-toluen-4-sulphonic acid 3-methyloxyranylmethyl ester
• Synonyms: (2R,3R)-toluen-4-sulphonic acid 3-methyloxyranylmethyl ester
• CAS NO: 107033-47-6
• Molecular Weight: 242.296
• Mol File: 107033-47-6.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: (2R,3R)-toluen-4-sulphonic acid 3-methyloxyranylmethyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: (2R,3R)-toluen-4-sulphonic acid 3-methyloxyranylmethyl ester(107033-47-6)
• EPA Substance Registry System: (2R,3R)-toluen-4-sulphonic acid 3-methyloxyranylmethyl ester(107033-47-6)

Safety Data

• Hazardous Substances Data: 107033-47-6(Hazardous Substances Data)

Upstream product

• 504-61-0 (E)-but-2-enol 
• 62961-64-2 D-(-)-diisopropyl tartrate 
• 98-59-9 p-toluenesulfonyl chloride 
• 58845-50-4 ((2R,3R)-3-methyloxiran-2-yl)methanol 
• 55058-23-6 (2R/3R)/(2S,3S)-2,3-epoxy-butanol 

Downstream Products

• 42969-65-3 (R)-(+)-3-butyn-2-ol 
• 143693-24-7 (R/S)-1,2-Butandiol-1-<(4-methylbenzol)sulfonat> 
• 132177-81-2 Toluene-4-sulfonic acid (2R,3S)-6-(tert-butyl-dimethyl-silanyloxy)-8,8-diethoxy-2-hydroxy-3-methyl-oct-4-ynyl ester 
• 132150-05-1 Toluene-4-sulfonic acid (2R,3S)-6-(tert-butyl-dimethyl-silanyloxy)-2-hydroxy-3-methyl-non-4-ynyl ester 

Relevant articles and documents

An efficient asymmetric synthesis of the potent β-blocker ICI-118,551 allows the determination of enantiomer dependency on biological activity

A highly efficient, practical and flexible two-step asymmetric synthesis of the β2-selective β-blocker ICI 118,551 is reported, allowing an unambiguous determination of the dependency of biological activity with optical activity, revealing the S,S-enantiomer to be the most potent.

Halocyclization of Unsaturated Alcohols and Carboxylic Acids Using Bis(sym-collidine)iodine(I) Perchlorate

Reaction of I(collidine)2(1+) ClO4(1-) with unsaturated alcohols and carboxylic acids in dichloromethane at ambient temperature has afforded three- to seven-membered-ring iodoethers and four- to seven-membered-ring iodolactones, respectively, in moderate