1094621-93-8

Basic information

• Product Name: [2-(4-chloro-phenyl)thiazol-5-yl]methanol
• Synonyms: [2-(4-chloro-phenyl)thiazol-5-yl]methanol
• CAS NO: 1094621-93-8
• Molecular Weight: 225.699
• Mol File: 1094621-93-8.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: [2-(4-chloro-phenyl)thiazol-5-yl]methanol(CAS DataBase Reference)
• NIST Chemistry Reference: [2-(4-chloro-phenyl)thiazol-5-yl]methanol(1094621-93-8)
• EPA Substance Registry System: [2-(4-chloro-phenyl)thiazol-5-yl]methanol(1094621-93-8)

Safety Data

• Hazardous Substances Data: 1094621-93-8(Hazardous Substances Data)

Upstream product

• 1679-18-1 4-Chlorophenylboronic acid 
• 2521-24-6 4-chlorothiobenzamide 

Downstream Products

• 27149-26-4 2-(4-chlorophenyl)thiazole 
• 1262511-84-1 2-[2-(4-chloro-phenyl)-5-methyl-thiazol-4-yl]-4-(5-fluoro-pyridin-2-ylmethyl)cyclopentane-1,3-dione 
• 1262512-57-1 2-[2-(4-chloro-phenyl)-5-methyl-thiazol-4-yl]-4-[1-(5-fluoro-pyridin-2-yl)meth-(E)-ylidene]cyclopentane-1,3-dione 
• 1262512-55-9 2-[2-(4-chloro-phenyl)-5-methyl-thiazol-4-yl]-5-[(5-fluoro-pyridin-2-yl)hydroxy-methyl]-3-methoxy-cyclopent-2-enone 
• 1262511-81-8 2-[2-(4-chloro-phenyl)-5-methyl-thiazol-4-yl]-4-(tetrahydro-pyran-4-ylmethyl)cyclopentane-1,3-dione 
• 1262512-16-2 2-[2-(4-chloro-phenyl)-5-methyl-thiazol-4-yl]-4-[1-(tetrahydro-pyran-4-yl)meth-(E)-ylidene]cyclopentane-1,3-dione 
• 1262512-52-6 2-[2-(4-chloro-phenyl)-5-methyl-thiazol-4-yl]-3-methoxy-5-[1-(tetrahydro-pyran-4-yl)meth-(E)-ylidene]cyclopent-2-enone 
• 1262512-50-4 2-[2-(4-chloro-phenyl)-5-methyl-thiazol-4-yl]-3-methoxy-cyclopent-2-enone 
• 1262512-48-0 2-[2-(4-chloro-phenyl)-5-methyl-thiazol-4-yl]cyclopentane-1,3-dione 
• 1262512-46-8 3-[2-(4-chloro-phenyl)thiazol-5-ylmethoxy]cyclopent-2-enone 
• 1094621-94-9 5-chloromethyl-2-(4-chloro-phenyl)-thiazole 

Relevant articles and documents

Metal-Free Aerobic Oxidative Selective C-C Bond Cleavage in Heteroaryl-Containing Primary and Secondary Alcohols

A transition-metal-free aerobic oxidative selective C-C bond-cleavage reaction in primary and secondary heteroaryl alcohols is reported. This reaction was highly efficient and tolerated various heteroaryl alcohols, generating a carboxylic acid derivative and a neutral heteroaromatic compound. Experimental studies combined with density functional theory calculations revealed the mechanism underlying the selective C-C bond cleavage. This strategy also provides an alternative simple approach to carboxylation reaction.