71963-96-7

Basic information

• Product Name: 2-iodo-1-tosylhexane
• Synonyms: 2-iodo-1-tosylhexane
• CAS NO: 71963-96-7
• Molecular Weight: 366.263
• Mol File: 71963-96-7.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 2-iodo-1-tosylhexane(CAS DataBase Reference)
• NIST Chemistry Reference: 2-iodo-1-tosylhexane(71963-96-7)
• EPA Substance Registry System: 2-iodo-1-tosylhexane(71963-96-7)

Safety Data

• Hazardous Substances Data: 71963-96-7(Hazardous Substances Data)

Upstream product

• 98-59-9 p-toluenesulfonyl chloride 
• 824-79-3 sodium 4-methylbenzenesulfinate 
• 592-41-6 1-hexene 
• 7257-26-3 sodium p-toluenesulfinate tetrahydrate 
• 1950-78-3 p-toluenesulfonyl iodide 

Downstream Products

• 90633-60-6 1-[((E)-Hex-2-ene)-1-sulfonyl]-4-methyl-benzene 
• 188430-26-4 (E)-6-propyl-6-tosyl-4-nonene 
• 188430-23-1 (E)-1-methyl-4-(non-5-en-4-ylsulfonyl)benzene 
• 105465-39-2 2-(1-pyrrolidinyl)-1-tosylhexane 
• 71964-05-1 (E)-1-(hex-1-en-1-ylsulfonyl)-4-methylbenzene 
• 105235-57-2 (Z)-1-tosyl-1-hexene 

Relevant articles and documents

"Syn-Effect" in the Desulfonylation Reaction of α,α-Dialkylated (E)-Allylic Sulfones

It was found that the desulfonylation reaction of α,α-dialkylated (E)-allylic sulfones with a base preferentially affords the sterically unfavorable (Z)-alkadienes. The relative degree of the "syn-effect", which is herein defined as an effect which stabil

CONVENIENT METHODS FOR THE PREPARATION OF VINYLIC AND ALLYLIC SULFONES FROM ALKENES

1 or 2-p-Toluenesulfonyl(=tosyl)-1-alkenes were regioselectively prepared from 1-alkenes via iodosulfonization or sulfonylmercuration, respectively.Conversion of 1-tosyl-1-alkenes to the corresponding allylic sulfones, 1-tosyl-2-alkenes, was achieved by t