880-22-8

Basic information

• Product Name: benzyl 3-methylbut-2-en-1-yl sulfide
• Synonyms: benzyl 3-methylbut-2-en-1-yl sulfide
• CAS NO: 880-22-8
• Molecular Weight: 192.325
• Mol File: 880-22-8.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: benzyl 3-methylbut-2-en-1-yl sulfide(CAS DataBase Reference)
• NIST Chemistry Reference: benzyl 3-methylbut-2-en-1-yl sulfide(880-22-8)
• EPA Substance Registry System: benzyl 3-methylbut-2-en-1-yl sulfide(880-22-8)

Safety Data

• Hazardous Substances Data: 880-22-8(Hazardous Substances Data)

Upstream product

• 100-53-8 phenylmethanethiol 
• 164513-96-6 1,1-dimethyl-2-propenyl isobutyl carbonate 
• 115-18-4 2-methyl-3-buten-2-ol 
• 5331-36-2 methyl 3-(benzylthio)propanoate 
• 870-63-3 prenyl bromide 
• 829-95-8 4-hydroxy-4-methyl-1-phenyl-2-thiapentane 
• 57634-10-3 2-(3-methyl-but-2-enyl)-isothiourea; hydrochloride 
• 100-39-0 benzyl bromide 
• 882-37-1 4-benzylsulfanyl-2-methyl-butan-2-ol 

Downstream Products

• 1391759-16-2 ethyl 2-(benzylthio)-3,3-dimethylpent-4-enoate 
• 909-96-6 4,4,4',4'-tetramethyl-2,2'-diphenyl-octahydro-[2,2']bi[1,3]thiazinyl 
• 881-54-9 4,4-dimethyl-2-phenyl-[1,3]thiazinane 
• 32456-13-6 1-methylthio-1-phenyl-2,2-dimethyl-but-3-ene 
• 881-55-0 4,4-dimethyl-2-phenyl-5,6-dihydro-4H-[1,3]thiazine 
• 65597-76-4 C₁₉H₂₂S₂ 

Relevant articles and documents

Method of manufacturing compds. Allylnaphthol

PROBLEM TO BE SOLVED: To provide a production method of an allyl compound of carrying out the dehydration allylation of a substrate having S, C or N which is a nucleophilic atom, especially S under the presence of a catalyst system consisting of a catalyst precursor having a specific structure and a specific ligand. SOLUTION: The production method of allyl compounds comprises as follow. A catalyst precursor chosen from Formula (1) and Formula (2) and a ligand are mixed, or a catalyst precursor, an allyl alcohol, and a ligand are mixed, then allyl alcohols and a substrate are blended and made to react. The ligand is quinaldic acid or picolinic acid, and the substrate is thiols, thiocarboxylic acids or the like. [Ru(C5H5)(CH3CN)3]PF6(1). [Ru[C5(CH3)5](CH3CN)3]PF6(2). COPYRIGHT: (C)2012,JPOandINPIT

Catalytic activation of diazo compounds using electron-rich, defined iron complexes for carbene-transfer reactions

Carbene transfer: The electron-rich iron complex Bu4N[Fe(CO) 3(NO)] efficiently catalyzes different carbene-transfer reactions. Various diazo compounds can be used. The high stability of the employed iron complexes is demonstrated by the generation of the diazo reagent in situ and a sequential iron-catalyzed allylic sulfenylation/Doyle-Kirmse reaction. Copyright

Palladium-catalyzed insertion reactions of trimethylsilyldiazomethane

Palladium(II) salts catalyze the Kirmse reaction of allylsulfides with trimethylsilyldiazomethane (TMSD) to give homoallylsulfides. Similarly, TMSD can intercept ArPdX intermediates generated during Stille couplings to give benzhydryl derivatives. The yie