56075-36-6

Basic information

• Product Name: 1-(4-chlorophenyl)-2-(methylsulfonyl)diazene
• Synonyms: 1-(4-chlorophenyl)-2-(methylsulfonyl)diazene
• CAS NO: 56075-36-6
• Molecular Weight: 218.664
• Mol File: 56075-36-6.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 1-(4-chlorophenyl)-2-(methylsulfonyl)diazene(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(4-chlorophenyl)-2-(methylsulfonyl)diazene(56075-36-6)
• EPA Substance Registry System: 1-(4-chlorophenyl)-2-(methylsulfonyl)diazene(56075-36-6)

Safety Data

• Hazardous Substances Data: 56075-36-6(Hazardous Substances Data)

Upstream product

• 20277-69-4 sodium methansulfinate 
• 106-47-8 4-chloro-aniline 
• 17696-73-0 methylsulfinic acid 
• 2028-74-2 p-chlorobenzenediazonium chloride 

Downstream Products

• 17221-37-3 2-(4-chlorophenyl)furan 
• 42498-40-8 N-tert-butyl-4-chlorobenzamide 
• 71320-77-9 moclobemide 
• 1229-73-8 (2-(4-chlorophenyl)ethene-1,1-diyl)dibenzene 
• 195062-61-4 4-chlorophenylboronic acid pinacol ester 
• 6113-62-8 2-(4-chlorophenyl)benzo[d][1,3,2]dioxaborole 
• 123-09-1 4-chlorophenyl methyl sulfide 
• 35921-85-8 benzyl (4-chlorophenyl) selenide 
• 154927-56-7 4-chlorophenyl 4’-methylphenyl selenide 
• 94800-51-8 (4-chlorophenyl)(phenyl)selane 
• 40640-46-8 2-(2-(4-chlorophenyl)hydrazono)-5,5-dimethylcyclohexane-1,3-dione 
• 24756-07-8 3-(4-chlorophenylhydrazono)-2,4-pentanedione 
• 3708-04-1 2-methylsulfonyl-1-phenylethanone 
• 14064-15-4 (4-chlorophenyl)trimethylstannane 

Relevant articles and documents

Additive- and Photocatalyst-Free Borylation of Arylazo Sulfones under Visible Light

We developed a photocatalyst-free and additive-free, visible light induced borylation reaction using arylazo sulfones as starting material. This protocol shows some advantages such as mild conditions, simple equipment, and wide substrate scope, which gives a complementary protocol for the preparation of arylboronates.

Visible-Light-Driven Synthesis of Arylstannanes from Arylazo Sulfones

The visible-light-driven preparation of (hetero)aryl stannanes was carried out under both photocatalyst- and metal-free conditions via irradiation of arylazo sulfones in the presence of hexaalkyldistannanes. The reaction shows a high efficiency and a wide substrates scope. The resulting crude organotin derivatives can be directly employed in a Stille protocol.