40296-93-3

Basic information

• Product Name: Benzene, (2-methyl-2-butenyl)-
• CAS NO: 40296-93-3
• Molecular Formula: C11H14
• Molecular Weight: 146.232
• Mol File: 40296-93-3.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: Benzene, (2-methyl-2-butenyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzene, (2-methyl-2-butenyl)-(40296-93-3)
• EPA Substance Registry System: Benzene, (2-methyl-2-butenyl)-(40296-93-3)

Safety Data

• Hazardous Substances Data: 40296-93-3(Hazardous Substances Data)

Upstream product

• 83659-69-2 3-methyl-3-nitro-4-phenyl-1-butene 
• 103-79-7 1-phenyl-acetone 
• 1754-88-7 ethylenetriphenylphosphorane 
• 97-94-9 triethyl borane 
• 152959-29-0 (+/-)-1-phenyl-2-(phenylsulfonyl)propane 
• 1009-62-7 2,2-dimethyl-3-phenylpropionaldehyde 
• 83565-90-6 C₁₇H₁₉NO₃S 
• 17322-34-8 (2-nitropropyl)benzene 
• 121368-72-7 erythro-2-Ethyl-3-hydroxy-2-methyl-3-phenylpropionic Acid 
• 42528-14-3 4-Chloro-1-phenyl-2-methyl-2-butene 
• 14389-04-9 tosylhydrazone of 2,2-dimethyl-3-phenylpropen-1-al 
• 772-46-3 2-methyl-1-phenyl-2-butanol 
• 13351-61-6 2,2-dimethyl-3-phenyl-1-propanol 

Downstream Products

• 61777-11-5 3-Aethyl-4-phenyl-penten-2 
• 61777-10-4 2-Isopropyl-3-phenyl-buten-1 
• 61777-12-6 2-Aethyl-3-methyl-1-phenyl-buten-1 
• 61777-09-1 3-Methyl-4-phenyl-2-penten 
• 64-19-7 acetic acid 
• 103-79-7 1-phenyl-acetone 

Relevant articles and documents

Preparation of alcohols from sulfones and trialkylboranes

The reaction of sulfone anions with trialkylboranes followed by thermal isomerization of the obtained boron compounds in the presence of excess borane-methyl sulfide complex and by alkaline hydroperoxide oxidation yields primary alcohols.

DENITROHYDROGENATION OF ALIPHATIC NITRO COMPOUNDS AND A NEW USE OF ALIPHATIC NITRO COMPOUNDS AS RADICAL PRECURSORS

Aliphatic nitro groups are replaced by hydrogen on treatment with tributyltin hydride which proceeds via free radical chain processes.As the nitro group is selectively denitrated and other reducible groups are not affected with tributyltin hydride, this reaction can be used as a method for removing the nitro group from polyfunctional compounds.The radical intermediates generated via denitration can be also used for the carbon-carbon bond forming reactions.