13865-07-1

Basic information

• Product Name: Benzene, [(methoxyphenylmethyl)thio]-
• CAS NO: 13865-07-1
• Molecular Formula: C14H14OS
• Molecular Weight: 230.331
• Mol File: 13865-07-1.mol
• Article Data: 10

Chemical Properties

• CAS DataBase Reference: Benzene, [(methoxyphenylmethyl)thio]-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzene, [(methoxyphenylmethyl)thio]-(13865-07-1)
• EPA Substance Registry System: Benzene, [(methoxyphenylmethyl)thio]-(13865-07-1)

Safety Data

• Hazardous Substances Data: 13865-07-1(Hazardous Substances Data)

Upstream product

• 67-56-1 methanol 
• 831-91-4 Benzyl phenyl sulfide 
• 591-50-4 iodobenzene 
• 13865-50-4 methoxymethyl phenyl sulfide 
• 1125-88-8 benzaldehyde dimethyl acetal 
• 108-98-5 thiophenol 
• 17314-33-9 tributyltin phenyl sulfide 
• 4551-15-9 phenylthiotrimethylsilane 

Downstream Products

• 22039-97-0 4-methoxy-4-phenyl-1-butene 
• 54322-72-4 (1-chlorobut-3-en-1-yl)benzene 
• 7695-69-4 bis(phenylthio)methylbenzene 
• 21213-27-4 phenyl 1-phenyl-3-butenyl sulfide 
• 121486-61-1 C₁₇H₁₈S 
• 52149-13-0 (1-Methoxy-2-methyl-but-3-enyl)-benzene 

Relevant articles and documents

Direct and indirect electrochemical generation of alkoxycarbenium ion pools from thioacetals

Thioacetals were found to be effective precursors to generate and accumulate alkoxycarbenium ions based on direct and indirect cation pool methods. Alkoxycarbenium ions thus generated reacted with carbon nucleophiles such as allylsilanes and enol silyl et

Lithium bromide, a novel and highly effective catalyst for monothioacetalization of acetals under mild reaction conditions

Lithium bromide is efficient as a catalyst for the monothioacetalization of acetals under mild reaction conditions to provide products in excellent yields with high chemoselectivity.

Unprecedented polymer-supported π-acid: Synthesis and its application as a promoter to the monothioacetalization of acetals

A novel polymer was synthesized by copolymerization of styrene monomer bearing dicyanoketene acetal functionality and ethylene glycol dimethacrylate, and used successfully as a recyclable π-acid catalyst in monothioacetalization of aromatic, aliphatic, acyclic, and cyclic acetals with thiophenol and phenylthiotrimethylsilane.