102154-41-6

Basic information

• Product Name: 2-(STYRYLSULFONYL)ACETIC ACID
• Synonyms: 2-(STYRYLSULFONYL)ACETIC ACID;2-(Styrylsulphonyl)acetic acid
• CAS NO: 102154-41-6
• Molecular Formula: C10H10O4S
• Molecular Weight: 226.25
• Mol File: 102154-41-6.mol

Chemical Properties

• Boiling Point: 504.8°Cat760mmHg
• Flash Point: 259.1°C
• Appearance: /
• Density: 1.391g/cm³
• Vapor Pressure: 5.18E-11mmHg at 25°C
• Refractive Index: 1.6
• CAS DataBase Reference: 2-(STYRYLSULFONYL)ACETIC ACID(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(STYRYLSULFONYL)ACETIC ACID(102154-41-6)
• EPA Substance Registry System: 2-(STYRYLSULFONYL)ACETIC ACID(102154-41-6)

Safety Data

• Hazardous Substances Data: 102154-41-6(Hazardous Substances Data)

Usage

InChI:InChI=1/C10H10O4S/c11-10(12)8-15(13,14)7-6-9-4-2-1-3-5-9/h1-7H,8H2,(H,11,12)/b7-6+

Upstream product

• 13435-97-7 styrylmercapto-acetic acid 
• 52147-97-4 trans 2-phenylethenesulfonyl chloride 
• 79-11-8 chloroacetic acid 
• 100-42-5 styrene 
• 1914-61-0 (Z)-Styrylthioacetic acid 
• 125065-59-0 methyl styrylthioacetate 
• 536-74-3 phenylacetylene 
• 7722-84-1 dihydrogen peroxide 
• 125065-60-3 Ethyl <(Z)-(2-phenylvinyl)sulfanyl>acetate 

Downstream Products

• 1038996-87-0 E-styrylsulfonylacetic acid methyl ester 
• 1595281-76-7 2-((phenylaminosulfonyl)methyl)-5-((3'-phenyl-5'-phenylisoxazol-4'-ylsulfonyl)methyl)-1,3,4-oxadiazole 
• 1595281-73-4 2-((phenylaminosulfonyl)methyl)-5-((1',3'-diphenyl-5'-phenyl-1'H-pyrazol-4'-ylsulfonyl)methyl)-1,3,4-oxadiazole 
• 1595281-70-1 2-((phenylaminosulfonyl)methyl)-5-((4',5'-dihydro-3'-phenyl-5'-phenylisoxazol-4'-ylsulfonyl)methyl)-1,3,4-oxadiazoles 
• 1595281-67-6 2-((phenylaminosulfonyl)methyl)-5-((4',5'-dihydro-1',3'-diphenyl-5'-phenyl-1'H-pyrazol-4'-ylsulfonyl)methyl)-1,3,4-oxadiazole 

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 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 and antioxidant activity of oxazolyl/thiazolylsulfonylmethyl pyrazoles and isoxazoles

A new class of oxazolyl/thiazolylsulfonylmethyl pyrazoles (10-13) and isoxazoles (14, 15) were prepared from the synthetically vulnerable intermediate E-styrylsulfonylacetic acid methyl ester (1) and studied their antioxidant activity.

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