118631-44-0

Basic information

• Product Name: 2-bromo-1-phenyl-nonan-1-one
• Synonyms: 2-bromo-1-phenyl-nonan-1-one
• CAS NO: 118631-44-0
• Molecular Weight: 311.262
• Mol File: 118631-44-0.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 2-bromo-1-phenyl-nonan-1-one(CAS DataBase Reference)
• NIST Chemistry Reference: 2-bromo-1-phenyl-nonan-1-one(118631-44-0)
• EPA Substance Registry System: 2-bromo-1-phenyl-nonan-1-one(118631-44-0)

Safety Data

• Hazardous Substances Data: 118631-44-0(Hazardous Substances Data)

Upstream product

• 104-72-3 decylbenzene 

Downstream Products

• 319482-19-4 3,8-diphenyl-2,7-dioctyl-difurano[2,3-a:2',3'-f]naphthalene 
• 319482-12-7 1,5-bis(1-phenyl-nonan-1-one-2-yloxy)-naphthalene 
• 13367-81-2 10-methylacridinium cation 
• 6048-82-4 decanophenone 
• 126583-81-1 2-Bromo-1-phenyl-decan-1-ol 

Relevant articles and documents

Silica sulfuric acid-promoted deacylation of α-bromo-β-diketones

Novel deacylation of α-bromo-β-diketones using silica sulfuric acid (SSA) has been developed. Deacylation of 3- bromopentane-2,4-diones and 2-bromobutane-1,3-diones were carried out in the presence of SSA in dichloroethane under mild conditions to obtain the corresponding α-bromo ketones in good to excellent yields. SSA also promoted the FriedelCrafts type alkylation of benzene with 3-(sec-alkyl)-2,4-pentanediones to give the corresponding triarylmethanes in high yields in benzene.

Direct synthesis of α-bromoketones from alkylarenes by aerobic visible light photooxidation

The direct synthesis of α-bromoketones from alkylarenes by aerobic photooxidation with hydrobromic acid is reported. The key success for this direct oxidative reaction is due to control of bromination with acetic acid and ethanol, which are generated in situ by solvolysis of ethyl acetate in the course of the reaction.