49639-22-7

Basic information

• Product Name: 1-Propanol, 3-(phenylsulfinyl)-
• CAS NO: 49639-22-7
• Molecular Formula: C9H12O2S
• Molecular Weight: 184.259
• Mol File: 49639-22-7.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: 1-Propanol, 3-(phenylsulfinyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: 1-Propanol, 3-(phenylsulfinyl)-(49639-22-7)
• EPA Substance Registry System: 1-Propanol, 3-(phenylsulfinyl)-(49639-22-7)

Safety Data

• Hazardous Substances Data: 49639-22-7(Hazardous Substances Data)

Usage

Physical state

Colorless, oily liquid

Odor

Faint

Uses

Solvent, intermediate in the production of other chemicals, synthesis of pharmaceuticals and agrochemicals

Potential applications

Organic chemistry

Reactivity

Can react with other compounds to form new chemical products

Handling precautions

Can be hazardous if not used and stored properly

Upstream product

• 24308-28-9 1,3-propanesultine 
• 24536-40-1 3-phenylthiopropanol 

Downstream Products

• 177416-13-6 phenyl 1,1-dideutero-3-hydroxypropyl sulfide 
• 112076-82-1 3-Benzenesulfinyl-3-chloro-propan-1-ol 
• 177416-28-3 phenyl 1,1-dideutero-3-hydroxypropyl sulfoxide 
• 33451-05-7 ((3-bromopropyl)sulfonyl)benzene 
• 19432-96-3 3-(phenylsulfonyl)propyl chloride 

Relevant articles and documents

Sulfoxide and sulfone compounds, as well as selective synthesis method and application thereof

The invention discloses a method for selectively synthesizing a sulfoxide compound shown as a formula (II) and a sulfone compound shown as a formula (III). In a reaction solvent, thioether (I) is usedas a reaction raw material and oxygen as an oxidation reagent, under the catalytic action of visible light and a photosensitive reagent; under the assistance of an additive, when a large-polarity proton-containing additive such as an acid and an alcohol or a solvent or an additive with excellent electron donating ability is used, a sulfoxide compound (II) is selectively generated; and when a small-polarity aprotic additive or a solvent is used, a sulfone compound (III) is selectively generated. The synthesis method has the advantages of easily available and cheap raw materials, simple reaction operation, mild reaction conditions, high yield and excellent functional group tolerance. According to the invention, synthesis and modification of some medicines are realized, and an efficient method for selectively constructing sulfoxide and sulfone compounds is provided for medicinal chemistry research.

Self-catalyzed oxidation of sulfides with hydrogen peroxide: A green and practical process for the synthesis of sulfoxides

A self-catalyzed selective oxidation of sulfides to sulfoxides has been developed. The scope of the protocol is demonstrated in the selective oxidation of 17 different substrates. High yields and chemoselectivity (in general > 90 % ) are achieved in most cases.

Formation of cyclic sulfonium salts by Me3SiI-promoted intramolecular displacement of hydroxide or methoxide by sulfide. Ring contraction thiepane → thiolane

A suitably positioned (1,2-, 1,4-, and 1,5-) intramolecular sulfide interferes with the iodotrimethylsilane-promoted iodine for hydroxyl substitution, as well as the related alcohol deprotection procedure (regioselective cleavage of methyl ethers). The ou