98821-28-4

Basic information

• Product Name: 2-P-TOLYL-ETHENESULFONYL CHLORIDE
• Synonyms: 2-P-TOLYL-ETHENESULFONYL CHLORIDE;(E)-2-(4-methylphenyl)ethylenesulfonyl chloride
• CAS NO: 98821-28-4
• Molecular Formula: C₉H₉ClO₂S
• Molecular Weight: 216.68
• Mol File: 98821-28-4.mol
• Article Data: 7

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 2-P-TOLYL-ETHENESULFONYL CHLORIDE(CAS DataBase Reference)
• NIST Chemistry Reference: 2-P-TOLYL-ETHENESULFONYL CHLORIDE(98821-28-4)
• EPA Substance Registry System: 2-P-TOLYL-ETHENESULFONYL CHLORIDE(98821-28-4)

Safety Data

• Hazardous Substances Data: 98821-28-4(Hazardous Substances Data)

Upstream product

• 104-87-0 4-methyl-benzaldehyde 
• 622-97-9 1-ethenyl-4-methylbenzene 

Downstream Products

• 37985-11-8 (E,E)-1-(4-methylphenyl)-4-phenylbuta-1,3-diene 
• 98821-18-2 (E)-2-chloro-2-phenylethyl p-methylstyryl sulfone 
• 155782-82-4 E-4-methylstyrylsulfonylacetic acid 
• 1350309-03-3 (E)-4-bromo-2-formylphenyl 2-p-tolylethenesulfonate 
• 1350309-26-0 6-bromo-3-(methoxy-(p-tolyl)methyl)-benzo[e][1,2]oxathiine-2,2-dioxide 
• 1350309-14-6 6-bromo-3-(4-methylbenzyl)benzo[e][1,2]oxathiin-4(3H)-one-2,2-dioxide 
• 1350309-13-5 8-methoxy-3-(4-methylbenzyl)benzo[e][1,2]oxathiin-4(3H)-one-2,2-dioxide 
• 1350309-02-2 (E)-2-formylphenyl 2-p-tolylethenesulfonate 
• 1350309-25-9 3-[methoxy(p-tolyl)methyl]benzo[e][1,2]oxathiine-2,2-dioxide 
• 1350309-12-4 3-(4-methylbenzyl)benzo[e][1,2]oxathiin-4(3H)-one-2,2-dioxide 
• 130828-76-1 1-Methyl-4-((1R,2S)-2-phenylmethanesulfonyl-cyclopropyl)-benzene 
• 130828-78-3 C₁₇H₁₇ClO₂S 
• 130828-79-4 C₁₇H₁₇ClO₂S 
• 130828-71-6 1-((E)-2-p-Tolyl-ethenesulfonylmethyl)-naphthalene 

Relevant articles and documents

Green approach for the synthesis of thiophenyl pyrazoles and isoxazoles by adopting 1,3-dipolar cycloaddition methodology and their antimicrobial activity

A variety of N-((1,3-diphenyl-5-aryl-1H-pyrazol-4-yl)sulfonyl)thiophene-2-carboxamides (7) and N-((5-aryl-3-phenylisoxazol-4-yl)sulfonyl)thiophene-2-carboxamides (8) were prepared from (E)-N-(arylethenesulfonyl)thiophene-2-carboxamides (4) adopting 1,3-di

Desulfonylation-Initiated Distal Alkenyl Migration in Copper-Catalyzed Alkenylation of Unactivated Alkenes

A novel and efficient protocol for desulfonylation-initiated distal alkenyl migration and its application to the elusive alkenylation of unactivated alkenes have been presented. This radical cascade process has successfully achieved the vicinal difluoroal

Tetrahydro-1,4-thiazine-1,1-dioxides: Part IV - Synthesis and conformational analysis of some 2,3,5-trisubstituted tetrahydro-1,4-thiazine-1,1-dioxides

A series of new 2-aroyl-3,5-diaryltetrahydro-1,4-thiazine-1,1-dioxides (2) has been synthesized either from phenacylsulfonylacetic acids (1) or phenacylstyrylsulfones (3), which in turn are obtained from the substituted acetophenones or styrenes, respecti