180639-95-6

Basic information

• Product Name: Phenol, 2-bromo-6-iodo-4-methyl-
• CAS NO: 180639-95-6
• Molecular Formula: C7H6BrIO
• Molecular Weight: 312.933
• Mol File: 180639-95-6.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: Phenol, 2-bromo-6-iodo-4-methyl-(CAS DataBase Reference)
• NIST Chemistry Reference: Phenol, 2-bromo-6-iodo-4-methyl-(180639-95-6)
• EPA Substance Registry System: Phenol, 2-bromo-6-iodo-4-methyl-(180639-95-6)

Safety Data

• Hazardous Substances Data: 180639-95-6(Hazardous Substances Data)

Upstream product

• 106-44-5 p-cresol 
• 6627-55-0 2-bromo-p-cresol 

Downstream Products

• 1335094-32-0 1-(5-methyl-2-phenylbenzo[b]furan-7-yl)piperidine 
• 1335094-33-1 1-(5-methyl-2-phenylbenzo[b]furan-7-yl)piperazine 
• 1335094-13-7 2-phenyl-5-methyl-7-bromobenzo[b]furan 
• 1422250-64-3 7-bromo-2-(4-methoxyphenyl)-5-methylbenzo[b]furan 
• 1422251-03-3 4-(2-(4-methoxyphenyl)-5-methylbenzo[b]furan-7-yl)morpholine 
• 1422250-92-7 (E)-5-fluoro-2-phenyl-7-styrylbenzo[b]furan 
• 1422250-86-9 2-methyl-4-(5-methyl-2-phenylbenzo[b]furan-7-yl)but-3-yn-2-ol 
• 1422250-84-7 4-(2-(4-methoxyphenyl)-5-methylbenzo[b]furan-7-yl)-2-methylbut-3-yn-2-ol 
• 1422250-82-5 7-((4-methoxyphenyl)ethynyl)-5-methyl-2-phenylbenzo[b]furan 
• 4789-95-1 3-Bromo-4-hydroxy-5-iodo-benzaldehyde 
• 87682-04-0 3,3'-Dibromo-5,5'-dimethyl<1,1'-biphenyl>-2,2'-diol 

Relevant articles and documents

Enhancing the synthetic utility of 3-haloaryne intermediates by their efficient Generation from readily synthesizable ortho-iodoaryl triflate-type precursors

Generation of 3-haloarynes from o-iodoaryl triflate-type precursors is reported. The method enables the generation of 3-fluorobenzyne with significantly high electrophilicity at -78 °C, allowing the formation of a three-component-coupled product between 3

2,5,7-Trisubstituted benzo[b]furans through a copper- and/or palladium-catalyzed assembly and functionalization process

A straightforward approach to the synthesis of 2,5,7-trisubstituted benzo[b]furans from 2-bromo- and 2-chloro-6-iodo-4-substituted phenols through a consecutive copper- and/or palladium-catalyzed assembly and functionalization process is described. Functionalization at the C(7) position is carried out by Suzuki-Miyaura cross-coupling and C-N bond forming reactions.