132731-64-7

Basic information

• Product Name: benzene
• Synonyms: benzene
• CAS NO: 132731-64-7
• Molecular Weight: 452.31
• Mol File: 132731-64-7.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: benzene(CAS DataBase Reference)
• NIST Chemistry Reference: benzene(132731-64-7)
• EPA Substance Registry System: benzene(132731-64-7)

Safety Data

• Hazardous Substances Data: 132731-64-7(Hazardous Substances Data)

Upstream product

• 591-50-4 iodobenzene 
• 3144-16-9 (1S)-10-camphorsulfonic acid 
• 3240-34-4 [bis(acetoxy)iodo]benzene 

Downstream Products

• 123541-43-5 3-((10-camphorsulfonyl)oxy)-4-phenylbutane-2,4-dione 
• 591-50-4 iodobenzene 
• 123541-42-4 3-((10-camphorsulfonyl)oxy)-2-butanone 
• 123541-41-3 1-((10-camphorsulfonyl)oxy)-2-butanone 
• 87456-38-0 2-((10-camphorsulfonyl)oxy)-1-phenyl-1-propanone 
• 87456-41-5 α-(camphorsulfonyloxy)acetophenone 

Relevant articles and documents

A novel camphorsulfonyloxylactonization of alkenoic acids

(Chemical Equation Presented) The novel reaction of [hydroxyl (((+)-10-camphorsulfonyl)oxy)iodo]benzene (1) with alkenoic acids was reported. When 1 reacted with various 4-pentenoic acids in CH3CN, camphorsulfonylactons were obtained in excellent yields in short times, some had two diastereoisomers, whereas 1 reacted with 5-hexenoic acid, giving middle yield of camphorsulfonylacton; however, 3-butenoic and trans-3-hexenoic acids reacted with 1 slowly in CH2Cl2, only unsaturated lactones were provided.

Facile one-pot preparation of [hydroxy(sulfonyloxy)iodo]arenes from iodoarenes with MCPBA in the presence of sulfonic acids

Various [hydroxy(sulfonyloxy)iodo]arenes were simply and efficiently obtained in high yields from the reaction of iodoarenes and MCPBA in the presence of sulfonic acids in a small amount of chloroform at room temperature, through a one-pot procedure. Georg Thieme Verlag Stuttgart.