23265-32-9

Basic information

• Product Name: 1-(METHYLSULFONYL)-2-PHENYLDIAZENE
• Synonyms: 1-(METHYLSULFONYL)-2-PHENYLDIAZENE
• CAS NO: 23265-32-9
• Molecular Formula: C₇H₈N₂O₂S
• Molecular Weight: 184.22
• Product Categories: Phenyls & Phenyl-Het;Phenyls & Phenyl-Het
• Mol File: 23265-32-9.mol
• Article Data: 8

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 1-(METHYLSULFONYL)-2-PHENYLDIAZENE(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(METHYLSULFONYL)-2-PHENYLDIAZENE(23265-32-9)
• EPA Substance Registry System: 1-(METHYLSULFONYL)-2-PHENYLDIAZENE(23265-32-9)

Safety Data

• Hazardous Substances Data: 23265-32-9(Hazardous Substances Data)

Upstream product

• 17696-73-0 methylsulfinic acid 
• 100-34-5 benzene diazonium chloride 
• 20277-69-4 sodium methansulfinate 
• 369-57-3 benzenediazonium tetrafluoroborate 
• 124-63-0 methanesulfonyl chloride 
• 100-63-0 phenylhydrazine 
• 110-00-9 furan 
• 2252-32-6 4-cyanophenyldiazonium tetrafluoroborate 
• 62-53-3 aniline 

Downstream Products

• 613-42-3 4-benzylbiphenyl 
• 25195-40-8 (methylsulfonyl)diphenylmethane 
• 606-97-3 2-benzyl-1,1'-biphenyl 
• 7466-42-4 4-phenylazobenzene 
• 5894-65-5 N-t-butylbenzamide 
• 2048-37-5 1-methyl-3-phenylquinoxalin-2(1H)-one (3a) 
• 1504-78-5 3-phenylquinoxaline-2(1H)-one 
• 88392-55-6 1-ethyl-3-phenylquinoxalin-2(1H)-one 
• 948-97-0 2,3-diphenyl-1-propene 
• 58-72-0 Triphenylethylene 
• 24388-23-6 2-phenyl-4,4,5,5-tetramethyl-1,3,2-dioxoborole 
• 100-68-5 methyl-phenyl-thioether 
• 622-38-8 Ethyl phenyl sulfide 
• 139-66-2 diphenyl sulfide 

Relevant articles and documents

-

-

SUBSTITUTED SULFONYL HYDRAZIDES AS INHIBITORS OF LYSINE BIOSYNTHESIS VIA THE DIAMINOPIMELATE PATHWAY

The present invention relates to substituted sulfonyl hydrazides that have the ability to inhibit lysine biosynthesis via the diaminopimelate pathway in certain organisms. As a result of this activity these compounds can be used in applications where inhibition of lysine biosynthesis is useful applications of this type include the use of the compound as herbicides and/or anti- bacterial agents.

Visible Light-Driven, Photocatalyst-Free Arbuzov-Like Reaction via Arylazo Sulfones

A visible light-induced formation of Aryl-Phosphorous bonds starting from arylazo sulfones and triaryl (or trialkyl)phosphites in the absence of any photoredox catalyst and any additives was developed. This reaction showed a broad substrate scope and afforded (hetero)aryl phosphonates in good yields and in up to the gram scale.