1613416-91-3

Basic information

• Product Name: (S)-(E)-4-cyclohexyl-2-(3-methoxyphenyl)but-3-ene-2-thiol
• Synonyms: (S)-(E)-4-cyclohexyl-2-(3-methoxyphenyl)but-3-ene-2-thiol
• CAS NO: 1613416-91-3
• Molecular Weight: 276.443
• Mol File: 1613416-91-3.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (S)-(E)-4-cyclohexyl-2-(3-methoxyphenyl)but-3-ene-2-thiol(CAS DataBase Reference)
• NIST Chemistry Reference: (S)-(E)-4-cyclohexyl-2-(3-methoxyphenyl)but-3-ene-2-thiol(1613416-91-3)
• EPA Substance Registry System: (S)-(E)-4-cyclohexyl-2-(3-methoxyphenyl)but-3-ene-2-thiol(1613416-91-3)

Safety Data

• Hazardous Substances Data: 1613416-91-3(Hazardous Substances Data)

Upstream product

• 1415351-65-3 (E,S)-S-4-cyclohexylbut-3-en-2-yl 1H-imidazole-1-carbothioate 
• 15378-40-2 trans-1-cyclohexyl-2-buten-1-one 
• 1613417-22-3 (S)-(E)-S-4-cyclohexyl-2-(3-methoxyphenyl)but-3-en-2-yl methylcarbamothioate 
• 79646-42-7 (2E,1R)-1-cyclohexyl-2-buten-1-ol 
• 1415351-95-9 (S)-(E)-S-4-cyclohexylbut-3-en-2-yl 3-methoxyphenyl(methyl)carbamothioate 
• 18736-82-8 1-cyclohexyl-but-2-en-1-ol 
• 79646-42-7 (E)-1-cyclohexyl-2-buten-1-ol 

Relevant articles and documents

Dihydrothiophenes containing quaternary stereogenic centres by sequential stereospecific rearrangements and ring-closing metathesis

Stereospecific [3,3]-sigmatropic rearrangement of O-substituted thiocarbamate derivatives of enantiopure allylic alcohols provides allylic thiocarbamates as single enantiomers. Intramolecular arylation by rearrangement of their allyllithium derivatives provides allylic tertiary thiols. Allylation and ring-closing metathesis gives 2,5-dihydrothiophenes containing sulfur-bearing quaternary centres. This journal is the Partner Organisations 2014.