58646-00-7

Basic information

• Product Name: (E)-N-(3-broMobenzylidene)propan-1-aMine
• Synonyms: (E)-N-(3-broMobenzylidene)propan-1-aMine
• CAS NO: 58646-00-7
• Molecular Formula: C₁₀H₁₂BrN
• Molecular Weight: 226.11298
• Mol File: 58646-00-7.mol
• Article Data: 4

Chemical Properties

• Boiling Point: 282.8±23.0 °C(Predicted)
• Appearance: /
• Density: 1.24±0.1 g/cm3(Predicted)
• PKA: 4.58±0.50(Predicted)
• CAS DataBase Reference: (E)-N-(3-broMobenzylidene)propan-1-aMine(CAS DataBase Reference)
• NIST Chemistry Reference: (E)-N-(3-broMobenzylidene)propan-1-aMine(58646-00-7)
• EPA Substance Registry System: (E)-N-(3-broMobenzylidene)propan-1-aMine(58646-00-7)

Safety Data

• Hazardous Substances Data: 58646-00-7(Hazardous Substances Data)

Usage

General Description

(E)-N-(3-bromobenzylidene)propan-1-amine is a chemical compound with the molecular formula C10H12BrN. It is an amine derivative with a benzylidene group and a bromo substituent. (E)-N-(3-broMobenzylidene)propan-1-aMine is often used in organic synthesis and pharmaceutical research as a reagent or intermediate. It possesses a chiral center and can exist as different stereoisomers, which may have different biological activities. Its structure and properties make it useful in the development of new drugs and as a building block in chemical reactions.

Upstream product

• 107-10-8 propylamine 
• 3132-99-8 m-bromobenzoic aldehyde 

Downstream Products

• 1262325-35-8 4-(3-bromobenzylidene)-2-methyl-1-propyl-1H-imidazol-5(4H)-one 
• 90389-92-7 N-(3-bromobenzyl)propylamine 

Relevant articles and documents

A latent reaction in a model GFP chromophore revealed upon confinement: Photohydroxylation of ortho -halo benzylidene-3-methylimidazolidiones via an electrocylization process

Excited state behavior of halogen substituted model GFP chromophores was investigated in an acetonitrile solution and in a confined environment provided by an octa acid capsule in water. Of the ortho, meta, and para halogen substituted GFP chromophores on

Separation of Ring Polar and Resonance Effects on the Rate Constants for Uncatalyzed N-Arylidenepropylamine Formation in Methanol

Rate constants are reported for the reaction of a series of 19 ring-substituted benzaldehydes with propylamine in methanol and in O-d-methanol at different temperatures and of three of them with 2-methoxyethylamine and 2,2-dimethoxyethylamine.The large di