5145-99-3

Usage

Uses

Used in the Food Industry:
Ethyl isopropyl sulfide is used as a flavoring agent to impart a garlic-like flavor to food products, enhancing their taste and aroma.
Used in the Gas Industry:
In the gas industry, ethyl isopropyl sulfide serves as an odorant in natural gas, providing a distinctive smell that aids in the detection of gas leaks, ensuring safety and preventing accidents.
Used in Organic Synthesis:
Ethyl isopropyl sulfide is utilized in organic synthesis due to its unique chemical properties, contributing to the development of new compounds and materials.
Used in Pharmaceutical Chemistry:
Its potential applications in pharmaceutical chemistry highlight the compound's versatility, as it may be involved in the synthesis of new drugs or serve as an intermediate in the production of existing medications.

InChI:InChI=1/C5H12S/c1-4-6-5(2)3/h5H,4H2,1-3H3

Upstream product

• 75-30-9 2-iodo-propane 
• 811-51-8 sodium thioethylate 
• 49774-03-0 dithiophosphoric acid O,O'-diethyl ester S-isopropyl ester 
• 20607-43-6 sodium isopropanethiolate 
• 75-03-6 ethyl iodide 
• 187737-37-7 propene 
• 108-24-7 acetic anhydride 
• 75-08-1 ethanethiol 
• 75-26-3 isopropyl bromide 

Downstream Products

• 4853-75-2 2-ethanesulfonyl-propane 
• 103375-95-7 C₁₂H₁₆N₂S*C₆H₃N₃O₇ 
• 103375-96-8 C₁₁H₁₆N₂O₂S*C₆H₃N₃O₇ 
• 103375-94-6 C₁₁H₁₆ClNS*C₆H₃N₃O₇ 

Relevant academic research and scientific papers

PROCESS FOR PREPARATION OF ALKYL SULFONE COMPOUNDS

An object of the present invention is to provide a method for preparation of an alkyl sulfone compound simply and safely with high yield, and an alkyl sulfone compound. The present invention is a method for preparing an alkyl sulfone compound represented by formula (2), comprising: oxidizing an alkyl sulfide compound represented by formula (1) using an oxidizing agent in the presence of a tungstate catalyst: in formula (1), R1 represents a C1-C3 alkyl group, and R2 represents a C3-C5 alkyl group, in formula (2), R1 and R2 are the same alkyl groups as R1 and R2 in formula (1), respectively.

Intermediacy of ion neutral complexes in the fragmentation of short-chain dialkyl sulfides

The main fragmentation processes after electron ionization of butyl methyl and butyl ethyl sulfides are rationalized by the intermediacy of the ion neutral complex [RSH · methylcyclopropane](+·) as demonstrated by extensive labeling and collision activation studies.

Alkyl- and Arylsulfenanilides by Cycloelimination of Propene from N-Aryl-S-isopropyl-sulfimides

A series of N-aryl-S-isopropyl-S-alkyl- or aryl-sulfimides has been prepared and transformed into alkyl- or arylsulfenanilides, respectively, by thermal cycloelimination of propene. - Keywords: Sulfimides; Sulfenanilides; Thermolysis; Cycloelimination.