909275-31-6

Basic information

• Product Name: 2-iodophenyl methoxymethyl sulfide
• Synonyms: 2-iodophenyl methoxymethyl sulfide
• CAS NO: 909275-31-6
• Molecular Weight: 280.129
• Mol File: 909275-31-6.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 2-iodophenyl methoxymethyl sulfide(CAS DataBase Reference)
• NIST Chemistry Reference: 2-iodophenyl methoxymethyl sulfide(909275-31-6)
• EPA Substance Registry System: 2-iodophenyl methoxymethyl sulfide(909275-31-6)

Safety Data

• Hazardous Substances Data: 909275-31-6(Hazardous Substances Data)

Upstream product

• 615-43-0 2-iodophenylamine 
• 140-89-6 potassium ethyl xanthogenate 
• 146335-10-6 1-bromo-2-<(methoxymethyl)thio>benzene 
• 6320-02-1 o-bromothiophenol 

Downstream Products

• 1610038-63-5 methoxymethyl 2-[(4-methylphenyl)ethynyl]phenyl sulfide 
• 1610038-64-6 2-[(4-fluorophenyl)ethynyl]phenyl methoxymethyl sulfide 
• 1610038-65-7 2-[(4-bromophenyl)ethynyl]phenyl methoxymethyl sulfide 
• 1610038-66-8 2-[(4-chlorophenyl)ethynyl]phenyl methoxymethyl sulfide 
• 1610038-67-9 C₁₄H₁₂OS₂ 
• 1610038-68-0 methoxymethyl 2-(4-phenylbut-1-yn-1-yl)phenyl sulfide 
• 1610038-69-1 2-(dec-1-yn-1-yl)phenyl methoxymethyl sulfide 
• 1610038-70-4 2-(cyclopropylethynyl)phenyl methoxymethyl sulfide 
• 1610038-51-1 bis[2-(2-phenylethyl)benzo[b]thiophen-3-yl]methanone 
• 937637-40-6 bis[2-(4-chlorophenyl)benzo[b]thiophen-3-yl]methanone 
• 1610038-48-6 bis[2-(4-fluorophenyl)benzo[b]thiophen-3-yl]methanone 
• 1610038-47-5 bis[2-(4-trifluoromethylphenyl)benzo[b]thiophen-3-yl]-methanone 
• 1610038-46-4 bis[2-(4-methoxyphenyl)benzo[b]thiophen-3-yl]methanone 
• 1610038-45-3 bis[2-(4-methylphenyl)benzo[b]thiophen-3-yl]methanone 

Relevant articles and documents

Gold-catalyzed intramolecular carbothiolation of alkynes: Synthesis of 2,3-disubstituted benzothiophenes from (α-alkoxy alkyl) (ortho-alkynyl phenyl) sulfides

(Chemical Equation Presented) Gold forms rings: AuCl-catalyzed cyclization of (α-alkoxy alkyl) (ortho-alkynyl phenyl) Sulfides 1 proceeds under mild conditions to give 3-(α-alkoxy alkyl) benzothiophenes 2 in high yields for a wide range of substrates (see