167390-74-1

Usage

General Description

2-Propenal, 2-[(phenylsulfonyl)methyl]- is a chemical compound that belongs to the family of aldehydes and ketones. It is also known as benzyl phenyl sulfone and has the molecular formula C10H10O3S. 2-Propenal, 2-[(phenylsulfonyl)methyl]- has a phenylsulfonylmethyl group attached to the aldehyde functional group, making it an important building block for the synthesis of various organic compounds. It is commonly used in organic chemistry as a reagent for the formation of carbon-carbon and carbon-hydrogen bonds, and it also has several industrial applications. Additionally, it is used as a key intermediate in the production of pharmaceuticals and agrochemicals. However, it is important to handle 2-Propenal, 2-[(phenylsulfonyl)methyl]- with care, as it can be toxic if not used appropriately.

Upstream product

• 401893-44-5 3-(phenylthio)-2-methylenepropionaldehyde diethyl acetal 
• 108-98-5 thiophenol 
• 57432-86-7 3-(phenylthio)propionaldehyde diethyl acetal 
• 27098-65-3 3-phenylsulfanyl-propionaldehyde 
• 117037-30-6 3-hydroxy 2-methylene propanesulfonyl benzene 

Downstream Products

• 117037-30-6 3-hydroxy 2-methylene propanesulfonyl benzene 
• 167390-73-0 C₁₀H₁₁⁽²⁾HO₃S 

Relevant academic research and scientific papers

Baker's yeast mediated biohydrogenation of sulphur-functionalised methacrolein derivatives. Stereochemical aspects of the reaction and preparation of the two enantiomers of useful C4 bifunctional chiral synthons

The baker's yeast mediated reduction of sulphur-functionalised methacroleins 11, 15 and 18 leads to the preparation of the bifunctional methyl branched C4 chiral synthons 6 and 7. The stereochemical aspects of the biohydrogenation have been investigated. Both the oxidation state of sulphur and the isomeric position of the double bond affected the enantioselectivity of the reduction strongly, thus, offering access to the two enantiomeric forms of 6 and 7.

Facile construction of substituted bicyclo [n.3.1] alkanones and the synthesis of a 12-membered dilactone via a new functionalized pentadienoic ester

4-Hydroxymethyl-2,4-pentadienoate was effectively synthesized and used for a synthetic entry to keto bridged bicyclo [n.3.1] alkanones and for the synthesis of a 12-membered macrodilide characterized by two trans double bonds, part of two vinylogous α-met