96227-77-9

Basic information

• Product Name: 1-((4-iodophenyl)diazenyl)piperidine
• Synonyms: 1-((4-iodophenyl)diazenyl)piperidine
• CAS NO: 96227-77-9
• Molecular Weight: 315.157
• Mol File: 96227-77-9.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: 1-((4-iodophenyl)diazenyl)piperidine(CAS DataBase Reference)
• NIST Chemistry Reference: 1-((4-iodophenyl)diazenyl)piperidine(96227-77-9)
• EPA Substance Registry System: 1-((4-iodophenyl)diazenyl)piperidine(96227-77-9)

Safety Data

• Hazardous Substances Data: 96227-77-9(Hazardous Substances Data)

Upstream product

• 110-89-4 piperidine 
• 540-37-4 p-aminoiodobenzene 

Downstream Products

• 1591-31-7 4-iodo-biphenyl 
• 326885-21-6 1-((4-iodophenyl)sulfonyl)piperidine 

Relevant articles and documents

Synthesis of triazene-substituted homoconjugated push-pull chromophores by formal [2?+?2] cycloadditions

1-(4-Ethynylphenyl)-3,3-dialkyltriaz-1-enes, well-known building blocks for branched dendrimer syntheses, were utilized as a new type of electron-donor component in formal [2 + 2] cycloadditions. The click-type, atom-economic reactions proceed efficiently

Catalytic conversion of aryl triazenes into aryl sulfonamides using sulfur dioxide as the sulfonyl source

Various sulfonamides have been synthesized from triazenes and sulfur dioxide. In the presence of just a catalytic amount of BF3· OEt2, a series of 1-aryl-triazenes were converted into sulfonyl hydrazines in good to excellent yields. When using CuCl2 as the catalyst, the corresponding sulfonamides can be produced from the 1-aryl triazenes in good yields. This journal is the Partner Organisations 2014.

Synthesis of Biaryls from Aryltriazenes

Aryltriazenes react with aromatic solvents in the presence of trifluoroacetic acid to produce biaryls.The mechanism of the reaction involves the formation of arenediazonium trifluoroacetates which lose nitrogen to give mainly aryl radicals.