65894-26-0

Basic information

• Product Name: Benzenemethanamine, N-(2-bromoethyl)-
• CAS NO: 65894-26-0
• Molecular Formula: C9H12BrN
• Molecular Weight: 214.105
• Mol File: 65894-26-0.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: Benzenemethanamine, N-(2-bromoethyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzenemethanamine, N-(2-bromoethyl)-(65894-26-0)
• EPA Substance Registry System: Benzenemethanamine, N-(2-bromoethyl)-(65894-26-0)

Safety Data

• Hazardous Substances Data: 65894-26-0(Hazardous Substances Data)

Upstream product

• 2576-47-8 2-bromoethylamine hydrobromide 
• 100-44-7 benzyl chloride 
• 100-39-0 benzyl bromide 

Downstream Products

• 151642-11-4 1-(2-benzylaminoethyl)-1H-imidazole 
• 103-55-9 N,N-dimethyl-N'-benzyl-1,2-ethanediamine 

Relevant articles and documents

Method for catalyzing aldol self-condensation reaction of low-carbon aldehyde by acid alkali double-function ionic liquid

The invention relates to a method for catalyzing aldol self-condensation reaction of low-carbon aldehyde by acid alkali double-function ionic liquid. The method comprises the following steps: adding low-carbon aldehyde and an acid alkali double-function ionic liquid catalyst into a high-pressure kettle, reacting at 60 to 150 DEG C for 1 to 12 hours, and performing hydroxyaldehyde self-condensationreaction on the low-carbon aldehyde to obtain long-chain unsaturated aldehyde, wherein the acid alkali double-function ionic liquid is the acid alkali double-function ionic liquid with cation and anion containing acid and alkali groups correspondingly, or the novel acid alkali double-function ionic liquid with cation containing acid and alkali groups. The method is applied to aldol self-condensation reaction of n-butanal and n-pentanal and is mild in reaction condition, high in catalytic activity and high in selectivity; and the acid alkali double-function ionic liquid catalyst can be reused.