1914-61-0

Usage

Uses

Used in Organic Synthesis:
(Z)-STYRYLTHIOACETIC ACID is used as a reagent in organic synthesis for [application reason], contributing to the creation of new chemical compounds and materials.
Used in Chemical Reactions:
In the field of chemical reactions, (Z)-STYRYLTHIOACETIC ACID is used as [application type] for [application reason], playing a crucial role in facilitating specific transformations and reactions.
Used in Pharmaceutical Industry:
(Z)-STYRYLTHIOACETIC ACID is used as a precursor in the synthesis of other organic compounds for [application reason], potentially leading to the development of new drugs and therapeutic agents.
Used in Research and Development:
In the research and development sector, (Z)-STYRYLTHIOACETIC ACID is used as [application type] for [application reason], such as studying its antimicrobial and anti-inflammatory properties, which could pave the way for novel applications in medicine and healthcare.
Used in Antimicrobial Applications:
(Z)-STYRYLTHIOACETIC ACID is used as an antimicrobial agent for [application reason], potentially offering a new approach to combat bacterial infections and contribute to the development of new antibiotics.
Used in Anti-inflammatory Applications:
As an anti-inflammatory agent, (Z)-STYRYLTHIOACETIC ACID is used for [application reason], which may include reducing inflammation and alleviating symptoms associated with various inflammatory conditions.

InChI:InChI=1S/C10H10O2S/c11-10(12)8-13-7-6-9-4-2-1-3-5-9/h1-7H,8H2,(H,11,12)/b7-6-

Upstream product

• 68-11-1 mercaptoacetic acid 
• 536-74-3 phenylacetylene 
• 125065-59-0 methyl styrylthioacetate 
• 125065-60-3 Ethyl <(Z)-(2-phenylvinyl)sulfanyl>acetate 

Downstream Products

• 92207-29-9 1-Methyl-4-[(E)-2-((Z)-2-phenyl-ethenesulfonyl)-vinyl]-benzene 
• 92207-26-6 1-Fluoro-4-[(E)-2-((Z)-2-phenyl-ethenesulfonyl)-vinyl]-benzene 
• 92207-25-5 (Z,E)-1-Chloro-4<2<(2-phenylethenyl)sulfonyl>ethenyl>-benzene 
• 92207-30-2 1-Methoxy-4-[(E)-2-((Z)-2-phenyl-ethenesulfonyl)-vinyl]-benzene 
• 92207-28-8 1-Nitro-2-[(E)-2-((Z)-2-phenyl-ethenesulfonyl)-vinyl]-benzene 
• 92207-27-7 1-Nitro-4-[(E)-2-((Z)-2-phenyl-ethenesulfonyl)-vinyl]-benzene 
• 92207-31-3 (Z)-styryl (E)-2-mehoxy-4-ethoxystyryl sulfone 
• 92207-24-4 (Z)-β-styrylsulfonylacetic acid 
• 125065-58-9 2-[(E)-2-((Z)-2-Phenyl-ethenesulfonyl)-vinyl]-naphthalene 
• 125065-56-7 1-Ethoxy-4-[(E)-2-((Z)-2-phenyl-ethenesulfonyl)-vinyl]-benzene 
• 125065-57-8 1-Isopropyl-4-[(E)-2-((Z)-2-phenyl-ethenesulfonyl)-vinyl]-benzene 
• 125065-54-5 1-Fluoro-3-[(E)-2-((Z)-2-phenyl-ethenesulfonyl)-vinyl]-benzene 
• 125065-55-6 1-Bromo-4-[(E)-2-((Z)-2-phenyl-ethenesulfonyl)-vinyl]-benzene 
• 65350-61-0 bis(2-phenylvinyl)sulfone 

Relevant academic research and scientific papers

Synthesis, antioxidant and anti-inflammatory activities of 5-((styrylsulfonyl) methyl)-1,3,4-oxadiazol / thiadiazol-2-amine derivatives

Background: A new class of 5-(styrylsulfonylmethyl)-1,3,4-oxadiazol-2-amine and 5- (styrylsulfonylmethyl)-1,3,4-thiadiazol-2-amine derivatives were prepared by derivatization of amino function. Methods: All the synthesized compounds were tested for antiox

Synthesis and antimicrobial activity of styryl/pyrrolyl/pyrazolyl sulfonylmethyl-1,3,4-oxadiazolyl amines and styryl/pyrrolyl/pyrazolyl sulfonylmethyl-1,3,4-thiadiazolyl amines

A new class of mono and bis heterocycles - styryl sulfonylmethyl-1,3,4-oxadiazolyl/1,3,4-thiadiazolyl amines, pyrrolyl sulfonylmethyl-1,3,4-oxadiazolyl/1,3,4-thiadiazolyl amines and pyrazolyl sulfonylmethyl-1,3,4-oxadiazolyl/1,3,4-thiadiazolyl amines were

Synthesis, antimicrobial and antioxidant activities of sulfone linked bis heterocycles - Pyrazolyl oxadiazoles and pyrazolyl thiadiazole

A new class of bis heterocycles - sulfone linked pyrazolyl oxadiazoles and thiadiazoles were developed from Z-styrylsulfonylacetic acid. The pyrazolyl thiadiazoles exhibited excellent antimicrobial activity whereas pyrazolyl oxadiazoles displayed good antioxidant activity.

Unsaturated thioacetic acids as novel mechanism-based inhibitors of peptidylglycine α-hydroxylating monooxygenase

Several unsaturated thioacetic acids were synthesized as potential mechanism-based inhibitors of peptidylglycine α-hydroxylating monooxygenase (PHM) prepared from horse serum. Trans-styrylthioacetic acid produced potent time-dependent inhibition of PHM. Potential mechanisms are proposed to explain PHM inactivation by unsaturated thioacetic acids.

THIOGLYCOLATES IN THE SYNTHESIS OF BIS(STYRYL)SULFONES

E,Z-Bis(styryl)sulfones (6), have been prepared by the Knoevenagel condensation of Z-styrylsulfonylacetic acid (5) with araldehydes.The compound 5 was prepared by a novel route using thioglycolates and phenylacetylene.The configuration of 6 has been assig