153046-39-0

Basic information

• Product Name: 4-Iodo-benzo[1,3]dioxole-5-carboxylic acid 2-(3-bromo-thiophene-2-carbonyloxy)-benzyl ester
• CAS NO: 153046-39-0
• Molecular Weight: 587.186
• Mol File: 153046-39-0.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 4-Iodo-benzo[1,3]dioxole-5-carboxylic acid 2-(3-bromo-thiophene-2-carbonyloxy)-benzyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: 4-Iodo-benzo[1,3]dioxole-5-carboxylic acid 2-(3-bromo-thiophene-2-carbonyloxy)-benzyl ester(153046-39-0)
• EPA Substance Registry System: 4-Iodo-benzo[1,3]dioxole-5-carboxylic acid 2-(3-bromo-thiophene-2-carbonyloxy)-benzyl ester(153046-39-0)

Safety Data

• Hazardous Substances Data: 153046-39-0(Hazardous Substances Data)

Upstream product

• 25796-68-3 3-bromo-thiophene-2-carbonyl chloride 
• 139058-83-6 4-Iodo-benzo[1,3]dioxole-5-carboxylic acid 2-hydroxy-benzyl ester 
• 133241-28-8 2-iodo-3,4-methylenedioxybenzoyl chloride 
• 90-01-7 salicylic alcohol 
• 7311-64-0 3-bromothiophene-2-carboxylic acid 

Relevant articles and documents

A FACILE SYNTHESIS OF HOGHLY FUNCTIONALIZED UNSYMMETRICAL HETEROBIARYLS UTILIZING THE INTRAMOLECULAR ULLMANN COUPLING REACTION DIRECTED BY SALICYL ALCOHOL AS A TEMPLATE

The cyclic heterobiaryls (3) containing a thenoyl of furoyl group were synthesized in good yields by regioselective acylations of salicyl alcohol (1), followed by the intramolecular Ullmann coupling reaction of the diesters (2).The cleavage of the two est