78751-36-7

Usage

Uses

Used in Polymer Synthesis:
2-(Thiobenzoylthio)propionic acid, Min. 97% is used as a RAFT agent for controlling the molecular weight and polydispersity of polymers. Its application in polymer synthesis allows for the production of polymers with well-defined structures and properties, which are essential for various industrial applications.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 2-(Thiobenzoylthio)propionic acid, Min. 97% is used as a building block for the synthesis of drug molecules. Its unique chemical structure enables the development of new therapeutic agents with improved efficacy and selectivity.
Used in Material Science:
2-(Thiobenzoylthio)propionic acid, Min. 97% is utilized in the development of advanced materials, such as polymers with specific mechanical, thermal, and electrical properties. These materials can be used in various applications, including electronics, automotive, and aerospace industries.
Used in Research and Development:
In research and development, 2-(Thiobenzoylthio)propionic acid, Min. 97% serves as a valuable tool for studying the fundamental aspects of polymerization reactions and the properties of the resulting polymers. This knowledge can be applied to design and develop new materials with tailored properties for specific applications.

Upstream product

• 3682-36-8 dithiobenzoic acid sodium salt 
• 598-72-1 2-Bromopropionic acid 
• 75-15-0 carbon disulfide 
• 108-86-1 bromobenzene 
• 474746-06-0 methyl 2-((phenylcarbonothioyl)thio)propanonate 
• 100-59-4 phenylmagnesium chloride 

Downstream Products

• 881212-56-2 succinimido-2-[[2-phenyl-1-thioxo]thio]-propanoate 
• 92126-28-8 2-methyl-5-phenyl-3,4-bis(hydroxymethyl)thiophene bis(methylcarbamate) 
• 20851-16-5 dimethyl 2-methyl-5-phenylthiophene-3,4-dicarboxylate 
• 92126-27-7 2-methyl-5-phenyl-3,4-bis(hydroxymethyl)thiophene 
• 881212-59-5 N-[8-((+)-biotinamido)-3,6-dioxaoctyl]-2-[[2-phenyl-1-thioxo]thio]propanamide 
• 881212-58-4 N-[6-desoxy-1,2:3,4-di-O-isopropylinene-6-α-D-galactopyranosyl]-2-[[2-phenyl-1-thioxo]thio]-propanamide 
• 881212-57-3 N-(2-morpholinoethyl)-2-[[2-phenyl-1-thioxo]thio]-propanamide 
• 20850-91-3 5-Methyl-2-phenyl-1,3-dithiolylium-4-olat 

Relevant academic research and scientific papers

Molecular weight and functional end group control by RAFT polymerization of a bisubstituted acrylamide derivative

Controlled radical polymerization of the bisubstituted acrylamide derivative N-acryloyl-morpholine (NAM) has the potential to yield telechelic polymers, one end of which can subsequently be grafted to latex particles. Once grafted, the other chain end of the polymer can be used as an immobilization site for species with applications in molecular biology and biomedicine. The controlled polymerization of NAM using reversible addition-fragmentation chain transfer (RAFT) is performed using two new chain transfer agents S = C(Z)-SR bearing the same functional propanoic acid group (R) and two different Z groups, benzyl (CTA 1) and phenyl (CTA 2). RAFT polymerization of NAM mediated by CTA 1 is very fast (>80% conversion in less than half an hour at 65 °C). The linear evolution of Mn and the low polydispersity indices (Mw/Mn a living polymerization. CTA 2 leads to broader Mw/Mn's (1H NMR and MALDI-ToF mass spectrometry.

CONTINUOUS FLOW SYNTHESIS OF DITHIOESTER COMPOUNDS

The present technology relates to methods of producing various dithioester-containing compounds via continuous flow reactors.

Versatile precursors of functional RAFT agents. Application to the synthesis of bio-related end-functionalized polymers

Biomolecule-polymer conjugates are widely used in bio-related fields, but their synthesis is often tricky, especially the introduction of a single biomolecule at one chain end. This paper describes a new straightforward approach to prepare such conjugates

Synthesis and evaluation of furan, thiophene, and azole bis[(carbamoyloxy)methyl] derivatives as potential antineoplastic agents

A series of bis(hydroxymethyl)-substituted heterocycles were synthesized and converted to the corresponding bis(methylcarbamate) derivatives. The heterocyclic systems studied were based on 2-phenyl-3-methylfuran, 1-phenylpyrazole, 1-phenyl-5-methylpyrazole, 1-phenyl-5-methylthiopene, 1-phenyl-1,2,3-triazole, 3-phenylisoxazole, 3-phenylisothiazole, 2-phenylthiazole, and 2-phenyloxazole. None of the bis(carbamates) prepared was active against murine P388 lymphocytic leukemia. Pyrrole bis(carbamate), which exhibited antileukemic activity, also showed reactivity toward 4-(p-nitrobenzyl)pyridine while the inactive bis(carbamates) were unreactive in the 4-(p-nitrobenzyl)pyridine assay.