85099-04-3

Usage

InChI:InChI=1/C7H16O2S/c1-2-3-4-10-6-7(9)5-8/h7-9H,2-6H2,1H3

Upstream product

• 29765-12-6 2-((n-butylthio)methyl)oxirane 
• 121033-53-2 2-Butylsulfanylmethyl-1,4,6-trioxa-spiro[4.4]nonane 
• 109-69-3 n-Butyl chloride 
• 96-27-5 rac-3-sulfanylpropane-1,2-diol 
• 109-79-5 n-butanethiol 
• 556-52-5 oxiranyl-methanol 

Downstream Products

• 143994-76-7 2-Butylsulfanylmethyl-1,4,7,10,13-pentaoxa-cyclopentadecane 

Relevant academic research and scientific papers

1,2-Diol type polyol derivative compound and preparation method thereof and anti-microbial composition containing it

The present invention relates to a polyol derivative compound having a 1,2-diol structure represented by chemical formula 1, a method of preparing the same, and an anti-microbial composition containing the compound as an active ingredient. In the chemical formula: R1 is nitrogen (N) or sulfur (S); and R2 is OH or C2 alkyl. According to the present invention, the polyol derivative compound having a 1,2-diol structure represented by the chemical formula 1 exhibits excellent anti-microbial activities better than 1,2-hexanediol, which is known to have the best anti-microbial activity among polyols, thereby being effectively used as a preservative for a food product, a medicine, a cosmetic, and the like to prevent spoilage caused by microorganisms.COPYRIGHT KIPO 2019

Facile Synthesis of Thiolariat Ethers or Crown Ethers Containing a Mercapto Group as a Side Arm

Cyclization reaction of S-substituted thioglycerol and oligoethylene glycol ditosylate gave thiolariat ethers in moderate yields.Mercaptomethyl crown ethers were obtained easily from benzylthiomethyl crown ethers by Na in liq.NH3-BuOH.

FUNCTIONALLY SUBSITUTED SULFUR-CONTAINING COMPOUNDS. 9. REASTIONS OF 2-OXIRANES WITH ACETIC ANHYDRIDE AND ACETYL CHLORIDE

Reaction of 2-oxiranes with acetic anhydride gives a mixture of 3-(organylthio)-1,2-diacetoxypropane and 2-(organylthio)-1,3-diacetoxypropane, and with acetyl chloride a mixture of 2-chloro-3-(organylthio)-1-acetoxypropane and 3-chloro-2-(organylthio)-1-acetoxypropane.In both cases, the ratio of the isomers depends on the nature of the organylthio group and on the nature of the electrophile.

RADICAL THIYLATION OF SOME UNSATURATED 1,3-DIOXOLANES

The radical addition of thiols to unsaturated 1,3-dioxolanes leads to the formation of the products from addition against the Markovnikov rule.Identical thioethers are produced as a result of nucleophilic substitution of the corresponding chloromethyl derivatives of 1,3-dioxolanes by sodium butanethiolate or phenylmethanethiolate.