53439-63-7

Upstream product

• 1569-69-3 Cyclohexanethiol 
• 106-95-6 allyl bromide 
• 107-05-1 3-chloroprop-1-ene 
• 107-18-6 allyl alcohol 
• 35466-83-2 allyl methyl carbonate 

Downstream Products

• 1569-69-3 Cyclohexanethiol 
• 89890-02-8 (Z)-2-(cyclohexylthio)-3-allyl-2-butene-1,4-diol 
• 89890-00-6 (E)-2-(cyclohexylthio)-3-allyl-2-butene-1,4-diol 
• 89890-06-2 (Z)-7-allyl-3,3,10,10-tetramethyl-6-(cyclohexylthio)-2,4,9,11-tetraoxa-6-dodecene 
• 89890-04-0 2,2-dimethyl-5-(cyclohexylthio)-6-allyl-4,7-dihydro-1,3-dioxepin 
• 254976-76-6 2-dibutylamino-1-methylethyl cyclohexyl sulfide 
• 254976-78-8 2-morpholino-1-methylethyl cyclohexyl sulfide 
• 254976-69-7 2-bromopropyl cyclohexyl sulfide 
• 89889-90-7 (E)-2-Allyl-3-cyclohexylsulfanyl-but-2-enedioic acid dimethyl ester 
• 89889-91-8 (Z)-2-Allyl-3-cyclohexylsulfanyl-but-2-enedioic acid dimethyl ester 

Relevant academic research and scientific papers

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

Highly efficient catalytic dehydrative S-allylation of thiols and thioic S-acids

A SH-selective allylation method using [CpRu(2-quinolinecarboxylato) (η3-C3H5)]PF6 has been realized in various solvents including aqueous media to give allyl sulfides and allyl S-thioates, demonstrating the potential applicability to lipopeptide chemistry.

Synthesis and properties of β- and γ-aminoalkyl sulfides

Reactions of mercaptans with allyl chloride, hydrobromination of the resulting allyl alkyl sulfides, and condensation of β-bromoalkyl sulfides with secondary amines were studied. The resulting β- and γ-aminoalkyl sulfides wre tested in gas treatment to re

Synthesis of organic sulfides using Ce-exchanged NaY catalyst

Synthesis of organic sulfides from thiols and alkyl halides is achieved using Ce-exchanged zeolite catalyst, Ce(72percent)NaY.