5891-07-6

Usage

Uses

Used in Pharmaceutical Synthesis:
2-(Propylamino)ethanethiol is used as a key intermediate in the synthesis of pharmaceuticals for its ability to contribute to the development of new drug molecules.
Used in Organic Chemistry:
As a reagent in organic chemistry, 2-(Propylamino)ethanethiol is employed to facilitate various chemical reactions, enhancing the efficiency and selectivity of the processes.
Used in Corrosion Inhibition:
2-(Propylamino)ethanethiol is used as a corrosion inhibitor to protect metal surfaces from degradation, extending the service life of equipment and structures in various industries.
Used in Plastics and Rubber Industry:
In the plastics and rubber industry, 2-(Propylamino)ethanethiol is used as a stabilizer to prevent the degradation of materials under various environmental conditions, ensuring the longevity and performance of the products.

Upstream product

• 420-12-2 thirane 
• 107-10-8 propylamine 
• 16982-46-0 2-ethyl-2-thiazoline 
• 5628-96-6 ethyl 2-mercaptoethyl carbonate 
• 60-29-7 diethyl ether 
• 5536-98-1 1-propylaziridine 

Relevant academic research and scientific papers

Syntheses de β-sultames (thiazetidines-1,2 dioxyde-1,1)

β-sultams (1,2-thiazetidine-1,1-dioxides) are easily prepared by 1-halogensulphonyl-2-aminoalkane cyclisation. Two processes based upon this principle have permitted the preparation of many variously N and C-substituted β-sultams. 1) In the first method 1-chlorosulphonyl-2-aminoalkane hydrochlorides, prepared from taurines or β-aminothiols, cyclised in the presence of base. 2) The second process involves the spontaneous cyclisation of 1-fluorosulphonyl-2-aminoalkanes prepared Michael addition of primary amines to 1-fluorosulphonylethene.

SYNTHESIS AND PROPERTIES OF β-SULTAMS

β-Sultames substituted in 2- and 3-position including bicyclic β-sultams were prepared and some of their reactions are reported.

Synthesis and radiopharmacological study of unsaturated derivatives of cysteamine

Synthesis of many unsaturated compounds derivated from cysteamine has been carried out in the three series : β-aminothioethers, β-aminothiols and thiazolidines. These products are more or less toxic, compared to corresponding saturated derivates. They generally have a higher radioprotective activity. The three most effective have a dose reduction factor equivalent to that of cysteamine, two of them having a lower toxicity.