139058-83-6

Basic information

• Product Name: 1,3-Benzodioxole-5-carboxylic acid, 4-iodo-, (2-hydroxyphenyl)methyl ester
• CAS NO: 139058-83-6
• Molecular Formula: C15H11IO5
• Molecular Weight: 398.154
• Mol File: 139058-83-6.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 1,3-Benzodioxole-5-carboxylic acid, 4-iodo-, (2-hydroxyphenyl)methyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: 1,3-Benzodioxole-5-carboxylic acid, 4-iodo-, (2-hydroxyphenyl)methyl ester(139058-83-6)
• EPA Substance Registry System: 1,3-Benzodioxole-5-carboxylic acid, 4-iodo-, (2-hydroxyphenyl)methyl ester(139058-83-6)

Safety Data

• Hazardous Substances Data: 139058-83-6(Hazardous Substances Data)

Upstream product

• 90-01-7 salicylic alcohol 
• 133241-28-8 2-iodo-3,4-methylenedioxybenzoyl chloride 

Downstream Products

• 153046-39-0 4-Iodo-benzo[1,3]dioxole-5-carboxylic acid 2-(3-bromo-thiophene-2-carbonyloxy)-benzyl ester 
• 133920-93-1 4-(4,5-Dimethoxy-2-o-tolyloxycarbonyl-phenyl)-benzo[1,3]dioxole-5-carboxylic acid 
• 139058-84-7 Benzo[1,3]dioxole-5-carboxylic acid 2-(3,4-dimethoxy-benzoyloxy)-benzyl ester 
• 133682-04-9 17-benzyloxy-16-methoxy-8H-benzo-1,3-benzodioxolo<4,5-e><1,8>benzodioxacycloundecin-6,14-dione 
• 133275-18-0 Dimethyl 5,6-methylenedioxy-4'-methoxy-5'-benzyloxy-2,2'-biphenyldicarboxylate 
• 133681-98-8 2-(2-iodo-3,4-methylenedioxybenzoyloxymethyl)phenyl 4-benzyloxy-2-iodo-5-methoxybenzoate 
• 145914-37-0 4-Iodo-benzo[1,3]dioxole-5-carboxylic acid 2-(2-iodo-thiophene-3-carbonyloxy)-benzyl ester 
• 153046-38-9 4-Iodo-benzo[1,3]dioxole-5-carboxylic acid 2-(2-iodo-furan-3-carbonyloxy)-benzyl ester 
• 145914-38-1 4-Iodo-benzo[1,3]dioxole-5-carboxylic acid 2-(3-iodo-thiophene-2-carbonyloxy)-benzyl ester 
• 133241-29-9 2-iodo-3,4-methylenedioxybenzoic acid 2-[(2-iodo-4,5-dimethoxyphenyl)carbonyloxy]benzyl ester 

Relevant articles and documents

2,2'-Disubstituted biphenyls: Synthesis and suppressive effect against carbon tetrachloride-induced liver injury

2,2'-Disubstituted biphenyl compounds (1-15) were synthesized by using the Ullmann coupling reaction as a key step. The suppressive effect of these compounds against CCl4-induced liver injuries in mice was evaluated. An unsymmetrical biphenyl (

A new synthesis of unsymmetrical diphenic acid derivatives: Template-directed intramolecular Ullmann coupling reaction

Intramolecular Ullmann coupling reaction of the diesters (6, 9), which were prepared by regioselective acylation of salicyl alcohol by using the two different substituted 2-iodobenzoyl chlorides, afforded the unsymmetrical diphenic acid derivatives (7, 10