54235-69-7

Usage

Chemical structure

A dithiane ring with a carbonyl chloride group attached to the 2nd carbon

Reactivity

Highly reactive

Versatility

Versatile compound used in organic synthesis

Application

Conversion of alcohols to carbonyl compounds

Use in pharmaceuticals

Preparation of pharmaceutical intermediates

Use in agrochemicals

Preparation of agrochemicals

Functional group transformations

Efficient and selective transformations on various functional groups

Synthetic chemistry

Valuable tool in synthetic chemistry

Safety precautions

Highly corrosive and toxic; should be handled with caution

Upstream product

• 20461-89-6 1,3-dithiane-2-carboxylic acid 

Downstream Products

• 33927-41-2 2-carboxamide-1,3-dithiane 
• 7647-14-5 sodium chloride 

Relevant academic research and scientific papers

A new approach to 4,6-disubstituted-3,4-dihydropyran-2-ones by Domino Michael addition-cyclization reaction under PTC conditions

Domino Michael addition-cyclization reactions of α,β-unsaturated carbonyl compounds with activated 1,3-dithiane-2-carbothioate esters under solid-liquid phase transfer catalysis conditions provide 4,6-disubstituted-3,4-dihydropyran-2-one-3,3-dithioacetals

Stereoselective chemo-enzymatic approaches to the synthesis of C 2 1,3-dithiane-1,3-dioxide

Two enzyme-mediated methods are presented for the preparation of enantiomerically enriched C2 1,3-dithiane-1,3-dioxide. The first takes advantage of a trans stereoselective oxidation by NaIO4 of enantiomerically pure (R) 1,3-dithiane-1-oxide ob

3-(1,3-Dithian-2-yl)-4-cyclo-pentene-2-carboxylic acids, esters and amides

The invention relates to the stereoisomers of novel cyclopentene derivatives and to the preparation thereof. The cyclopentene derivatives are obtained by cycloaddition reaction between cyclopentadiene and a mono-or bis-thioalkyl (or aryl) ketene and r