1914-61-0

Basic information

• Product Name: (Z)-STYRYLTHIOACETIC ACID
• Synonyms: (Z)-STYRYLTHIOACETIC ACID
• CAS NO: 1914-61-0
• Molecular Formula: C₁₀H₁₀O₂S
• Molecular Weight: 0
• Mol File: 1914-61-0.mol
• Article Data: 7

Chemical Properties

• Appearance: /
• CAS DataBase Reference: (Z)-STYRYLTHIOACETIC ACID(CAS DataBase Reference)
• NIST Chemistry Reference: (Z)-STYRYLTHIOACETIC ACID(1914-61-0)
• EPA Substance Registry System: (Z)-STYRYLTHIOACETIC ACID(1914-61-0)

Safety Data

• Hazardous Substances Data: 1914-61-0(Hazardous Substances Data)

Usage

General Description

(Z)-STYRYLTHIOACETIC ACID is a chemical compound with the molecular formula C10H10O2S. It is a derivative of thioacetic acid and is typically found in the form of a white to off-white powder. (Z)-STYRYLTHIOACETIC ACID is used in the field of organic synthesis and as a reagent in chemical reactions. (Z)-STYRYLTHIOACETIC ACID has been studied for its potential biological activities, including its antimicrobial and anti-inflammatory properties. It has also been investigated for its potential use in pharmaceuticals and as a precursor in the synthesis of other organic compounds.

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

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

Downstream Products

• 92207-24-4 (Z)-β-styrylsulfonylacetic acid 
• 92207-31-3 (Z)-styryl (E)-2-mehoxy-4-ethoxystyryl sulfone 
• 92207-27-7 1-Nitro-4-[(E)-2-((Z)-2-phenyl-ethenesulfonyl)-vinyl]-benzene 
• 92207-28-8 1-Nitro-2-[(E)-2-((Z)-2-phenyl-ethenesulfonyl)-vinyl]-benzene 
• 92207-30-2 1-Methoxy-4-[(E)-2-((Z)-2-phenyl-ethenesulfonyl)-vinyl]-benzene 
• 92207-25-5 (Z,E)-1-Chloro-4<2<(2-phenylethenyl)sulfonyl>ethenyl>-benzene 
• 92207-26-6 1-Fluoro-4-[(E)-2-((Z)-2-phenyl-ethenesulfonyl)-vinyl]-benzene 
• 92207-29-9 1-Methyl-4-[(E)-2-((Z)-2-phenyl-ethenesulfonyl)-vinyl]-benzene 
• 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 articles and documents

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, 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.

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