123958-48-5

Upstream product

• 41967-53-7 4-formyl-1-(methylsulfenyl)methoxybenzene 

Downstream Products

• 123958-53-2 4-allyloxymethylphenyl methylthiomethyl ether 
• 133594-82-8 sodium 1-(4-acetoxymethylphenoxy)methyl-5-chloro-2-oxo-1,2,3,4-tetrahydropyrimidine-4-sulfonate 
• 133594-87-3 sodium 5-chloro-1-(4-hydroxymethylphenoxy)methyl-2-oxo-1,2,3,4-tetrahydropyrimidine-4-sulfonate 
• 133594-88-4 sodium 5-chloro-1-(4-hydroxymethylphenoxy)methyl-2-oxo-1,2,3,6-tetrahydropyrimidine-6-sulfonate 
• 133594-77-1 1-(4-acetoxymethylphenoxy)methyl-5-chloro-2(1H)-pyrimidinone 
• 133594-84-0 5-Chloro-1-(4-hydroxymethyl-phenoxymethyl)-1H-pyrimidin-2-one 
• 133594-72-6 4-acetoxymethyl-1-chloromethoxybenzene 
• 123958-54-3 4-propargyloxymethylphenyl methylthiomethyl ether 
• 133594-69-1 1-acetoxymethyl-4-methylthiomethoxybenzene 

Relevant academic research and scientific papers

Syntheses and studies of metaphase-arresting pyrimidinones.

Methods are described for the syntheses of chloromethyl hydroxyalkylphenyl and benzyl ethers, and for the synthesis of bromomethyl phenyl ketone analogs. The hydroxy groups were protected as acetates. The halogenomethyl derivatives have been used for N-al

Synthesis of Unsaturated Chloromethyl Ethers

Alkenyl or alkynyl chloromethyl ethers have been prepared from O,S-acetals by reaction with sulfuryl chloride in the presence of cyclohexene or a styrene as a trapping reagent for the sulfenyl halide which is formed in the reaction.Chloromethyl phenyl eth