20600-60-6

Usage

Uses

Used in Organic Synthesis:
(PROPYLTHIO)ACETIC ACID is used as a reagent for the preparation of various sulfur-containing compounds, playing a crucial role in the synthesis of organic molecules.
Used in Pharmaceutical Applications:
(PROPYLTHIO)ACETIC ACID is used as a potential antimicrobial and antifungal agent, indicating its potential in the development of new drugs to combat infections.
Used in Corrosion Inhibition:
(PROPYLTHIO)ACETIC ACID is used as a corrosion inhibitor, helping to protect materials from degradation in various industrial settings.
Used in Polymer Production:
(PROPYLTHIO)ACETIC ACID is used as a reagent in the production of polymers, contributing to the development of new materials with specific properties for different applications.

InChI:InChI=1/C5H10O2S/c1-2-3-8-4-5(6)7/h2-4H2,1H3,(H,6,7)

Upstream product

• 89794-71-8 ethyl (propylthio)acetate 
• 106-94-5 propyl bromide 
• 68-11-1 mercaptoacetic acid 
• 107-03-9 1-thiopropane 
• 1071-75-6 2-propyl-isothiourea; hydrobromide 
• 79-11-8 chloroacetic acid 

Downstream Products

• 20600-65-1 methyl (propylthio)acetate 
• 387398-24-5 4-Phenylethynyl-N-(2-(2-propylthioacetylamino)sulfonylphenyl]benzamide 
• 58992-40-8 (C₆H₅)3Bi(OOCCH₂S(n-C₃H₇))2 
• 636-70-4 triethylamine hydrobromide 

Relevant academic research and scientific papers

8-Chlorodibenz[b,f][1,4]oxazepine-10(11H)-carboxylic acid, 2-(sulfinyl- and sulfonyl-containing acyl)hydrazides

This invention relates to 8-chlorodibenz[b,f][1,4]oxazepine-10(11H)-carboxylic acid, 2-(sulfinyl- and sulfonyl-containing acyl)hydrazides that are useful as prostaglandin antagonists and analgesic agents.

Mass Spectrometry of 2-Alkylthio-2-methylpropanoic Acids and Their Esters and Amides. Structural and Steric Effects on the McLafferty Rearrangement

The electron ionization mass spectra (MS) of S-methylated derivatives of N-(2-mercapto-2-methylpropanoyl)-L-cysteine and 2-alkylthio-2-methylpropanoic acids, as well as their esters and amides, were examined.Use of the deuterium labeling technique and accurate mass measurement supported the proposed fragmentation pathways.Extensive loss of CH2S from a molecular ion by the McLafferty rearrangementof a primary hydrogen is important in the MS of S-methyl compounds of amide derivatives.It was demonstrated that the intensity of the rearrangement ion decreases in the order of amide, ester, and acid, and in the case if amides the reaarangement is suppressed by the nonbonded interaction between methyl groups on the α carbon and the amide nitrogen.Keywords-N-(2-mercapto-2-methylpropanoyl)-L-cysteine; 2-alkylthio-2-methylpropanoic acid and methyl ester; 2-alkylthio-2-methylpropanamide; electron impact mass spectrometry; McLafferty rearrangement; steric interaction