6331-20-0

Usage

Derivative of propanoic acid

2-(((benzylthio)carbonothioyl)amino)propanoic acid is derived from propanoic acid, which is a simple carboxylic acid with a three-carbon chain.

Carbonothioyl group

The presence of a carbonothioyl group (C=S) in the compound gives it unique chemical properties compared to its oxygen-containing counterpart, the carbonyl group (C=O).

Benzylthio group

The compound also contains a benzylthio group (C6H5SH), which is a thiol group attached to a benzene ring. This group imparts additional chemical reactivity and properties to the molecule.

Potential applications

2-(((benzylthio)carbonothioyl)amino)propanoic acid can be used in various fields, such as pharmaceuticals and organic synthesis, due to its unique chemical structure and properties.

Further research and testing

The specific chemical properties and potential applications of 2-(((benzylthio)carbonothioyl)amino)propanoic acid would depend on further research and testing in the laboratory, as its properties and uses are not yet fully understood.

Upstream product

• 302-72-7 rac-Ala-OH 
• 75-15-0 carbon disulfide 
• 100-44-7 benzyl chloride 

Relevant academic research and scientific papers

Amino Acid-Based Dithiocarbamates as Efficient Intermediates for Diversity-Oriented Synthesis of Thiazoles

Amino acid-based dithiocarbamates were introduced as efficient intermediates for the synthesis of a diverse library of novel di- and tri-substituted thiazoles via condensation with various reagents such as anhydrides, acyl halides, benzene sulfonyl chloride, trifluoromethanesulfonic anhydride, chloroethyl formate, and diethyl chlorophosphate. The utilities of adducts in further organic synthesis were confirmed by Sonogashira and oxidation reactions. In addition, reaction of aspartic acid-based dithiocarbamates with anhydrides affords the corresponding fused 6,6a-dihydrofuro[3,2-d]thiazol-5(3aH)-ones diastereoselectively in excellent yields.

Synthesis of a new series of dithiocarbamate-linked peptidomimetics and their application in Ugi reactions

Novel peptidomimetics containing dithiocarbamate groups were synthesized via the Ugi reaction. Also, dithiocarbamates of natural amino acids were prepared and were used successfully in Ugi reactions to prepare novel peptidomimetics bearing amino acid and dithiocarbamate groups in a single structure. In addition the prepared dithiocarbamates based on amino acids are converted to the corresponding amides.