326885-21-6

Basic information

• Product Name: 1-((4-iodophenyl)sulfonyl)piperidine
• Synonyms: 1-((4-iodophenyl)sulfonyl)piperidine
• CAS NO: 326885-21-6
• Molecular Weight: 351.208
• Mol File: 326885-21-6.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 1-((4-iodophenyl)sulfonyl)piperidine(CAS DataBase Reference)
• NIST Chemistry Reference: 1-((4-iodophenyl)sulfonyl)piperidine(326885-21-6)
• EPA Substance Registry System: 1-((4-iodophenyl)sulfonyl)piperidine(326885-21-6)

Safety Data

• Hazardous Substances Data: 326885-21-6(Hazardous Substances Data)

Upstream product

• 96227-77-9 1-((4-iodophenyl)diazenyl)piperidine 
• 110-89-4 piperidine 
• 540-37-4 p-aminoiodobenzene 
• 110-85-0 piperazine 
• 98-61-3 p-Iodobenzenesulfonyl chloride 

Downstream Products

• 1428626-94-1 C₁₇H₁₈ClNO₄S 
• 1428626-92-9 C₁₈H₂₀ClNO₄S 

Relevant articles and documents

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.

New phenylpyridylpiperazine compounds

A compound selected from those of formula (I): [image] wherein: X represents a C(O) or SO2 group, R1 represents an aryl group or a group NR3R4 wherein R3 and R4 are as defined in the description, R2 represents an alkyl, (C3-C8)cycloalkyl or (C3-C8)cycloalkyl-(C1-C6)alkyl group, its isomers, and addition salts thereof, and medicinal products containing the same which are useful in treating conditions treatable by antagonists of type H3 central histamine receptors.