187975-06-0

Basic information

• Product Name: 2-(1-methoxy-1-phenylmethyl)-4,5-dimethylthiazole
• Synonyms: 2-(1-methoxy-1-phenylmethyl)-4,5-dimethylthiazole
• CAS NO: 187975-06-0
• Molecular Weight: 233.334
• Mol File: 187975-06-0.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 2-(1-methoxy-1-phenylmethyl)-4,5-dimethylthiazole(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(1-methoxy-1-phenylmethyl)-4,5-dimethylthiazole(187975-06-0)
• EPA Substance Registry System: 2-(1-methoxy-1-phenylmethyl)-4,5-dimethylthiazole(187975-06-0)

Safety Data

• Hazardous Substances Data: 187975-06-0(Hazardous Substances Data)

Upstream product

• 100-52-7 benzaldehyde 
• 3581-91-7 4,5-Dimethylthiazole 
• 169899-58-5 2-(1-hydroxy-1-phenylmethyl)-4,5-dimethylthiazole 
• 74-88-4 methyl iodide 

Downstream Products

• 1403588-43-1 (Z)-2-(methoxy(phenyl)methylene)-3,4,5-trimethyl-2,3-dihydrothiazole 
• 1403588-55-5 (E)-2-(methoxy(phenyl)methylene)-3,4,5-trimethyl-2,3-dihydrothiazole 

Relevant articles and documents

NHC-Stabilized Radicals in the Formal Hydroacylation Reaction of Alkynes

Mechanistic details of transformations catalyzed by N-heterocyclic carbenes (NHC) are currently of great interest, targeting questions on the active catalyst in operation and the structure and reactivity of key intermediates. These mechanistic studies are

Kinetics of C(2α)-proton abstraction from 2-benzylthiazolium salts leading to enamines relevant to catalysis by thiamin-dependent enzymes

The kinetics of proton transfer from the C(2α) position of 2-(1-methoxybenzyl)thiazolium salts was studied for the p-H and p-N(CH3)3+ derivatives as models for the protonation of the enamine/C(2α)-carbanion, a key intermed