37488-40-7

Basic information

• Product Name: BENZYLAMINE HYDROBROMIDE
• Synonyms: BENZYLAMINE HYDROBROMIDE;Benzylammonium bromide
• CAS NO: 37488-40-7
• Molecular Formula: Br*C₇H₁₀N
• Molecular Weight: 107.1531
• Mol File: 37488-40-7.mol

Chemical Properties

• Melting Point: 204°C(lit.)
• Boiling Point: 185°Cat760mmHg
• Flash Point: 60°C
• Appearance: /
• Density: 0.979g/cm³
• Water Solubility: Soluble in water
• CAS DataBase Reference: BENZYLAMINE HYDROBROMIDE(CAS DataBase Reference)
• NIST Chemistry Reference: BENZYLAMINE HYDROBROMIDE(37488-40-7)
• EPA Substance Registry System: BENZYLAMINE HYDROBROMIDE(37488-40-7)

Safety Data

• Hazardous Substances Data: 37488-40-7(Hazardous Substances Data)

Usage

Uses

Used in Pharmaceutical Industry:
BENZYLAMINE HYDROBROMIDE is used as an intermediate in the synthesis of various pharmaceutical compounds for [application reason]. Its reactivity allows for the creation of a wide range of drugs with different therapeutic properties.
Used in Chemical Synthesis:
BENZYLAMINE HYDROBROMIDE is used as a reagent in chemical synthesis for [application reason]. Its ability to form salts and react with other compounds makes it a versatile building block for creating new molecules with specific functions.
Used in Research and Development:
BENZYLAMINE HYDROBROMIDE is used as a research compound for [application reason]. It is often utilized in laboratories to study its properties and to develop new methods for synthesizing related compounds or understanding its interactions with other molecules.
Used in Solar Cell Applications:
BENZYLAMINE HYDROBROMIDE is used as a precursor in the synthesis of organohalide-based perovskites for [application reason]. These perovskites are important materials for optimizing the band gap, carrier diffusion length, and power conversion efficiency of perovskite-based solar cells.

Upstream product

• 33280-23-8 N-(4-chlorophenyl)-N-methyl-2-bromoacetamide 
• 100-46-9 benzylamine 
• 623-08-5 N-methyl-p-toluidine 
• 23543-31-9 2-bromo-N-methyl-N-(4-nitrophenyl)acetamide 
• 29182-97-6 N-methyl-2-bromoacetanilide 
• 1319751-61-5 N-methyl-4-methyl-α-bromoacetanilide 
• 948551-23-3 2-bromo-N-(4-methoxyphenyl)-N-methylacetamide 
• 79343-93-4 1-ethyl-2-bromo-pyridinium; bromide 
• 29636-75-7 3-bromo-1-phenylpropan-1-one 
• 1884-29-3 ethyl 2-bromo-3-phenyl-propionate 

Downstream Products

• 68263-59-2 N-benzylnonaneamide 
• 2403-22-7 N-Benzyl-N-butylamine 
• 4383-27-1 N,N-di-n-butylbenzylamine 
• 64892-53-1 N-benzylalanine ethyl ester 
• 23574-01-8 3-benzylamino-propionic acid methyl ester 
• 793-19-1 bis(2-methoxycarbonylethyl)benzylamine 
• 3647-71-0 N-benzyl-2-phenylethylamine 
• 76842-47-2 N-benzyl-N-phenylethyl-2-phenylethanamine 
• 22643-20-5 N-benzyl-N-octyloctan-1-amine 
• 1667-16-9 N-benzyl-N-octylamine 
• 102629-61-8 bis(benzylammonium) tetrabromochromate(II) 
• 538-32-9 benzylurea 
• 100-52-7 benzaldehyde 

Relevant articles and documents

Nucleophilic substitution reactions of N-methyl α-bromoacetanilides with benzylamines in dimethyl sulfoxide

Kinetic studies of the reactions of N-methyl-Y-a-bromoacetanilides with substituted X-benzylamines have been carried out in dimethyl sulfoxide at 25.0 °C. The Hammett plots for substituent X variations in the nucleophiles (log kN vs σX) are slightly bipha

KINETICS AND MECHANISM OF REACTION OF AMINES WITH β-BROMOPROPIOPHENONE

The reaction of β-bromopropiophenone with different amines in acetonitrile at 25 deg C was studied.It was found that in the case of primary and secondary amines, the end products of the reaction are β-aminopropiophenones, which form via the intermediate phenyl vinyl ketone.In the case of tertiary amines, the reaction ends at the stage of the formation of phenyl vinyl ketone.The reactivity of the amines in the formation of phenyl vinyl ketone is preferentially determined by their basicity.

KINETICS OF THE REACTIONS OF 2-HALOGENOPYRIDINIUM SALTS WITH PRIMARY AND SECONDARY AMINES IN ACETONITRILE

The kinetics of the reactions of 2-halogeno-N-alkylpyridinium salts with primary and secondary aliphatic amines in acetonitrile at 25 deg C were investigated.The reactions obey second-order relationships.In the reaction of 2-bromo-N-ethylpyridinium bromide with aliphatic amines the effect of electronic and steric factors on the reactivity of the amines was examined.

Carboxyl terminated polydienes

Carboxyl terminated polymers prepared by reacting a cyclic anhydride with a liquid polymeric hydroxyl terminated polymer selected from polyethers, polydienes, and copolymers of the dienes with styrene or acrylonitrile in the presence of a catalyst selected from quaternary ammonium salts and from halogen acid salts of amines. The carboxyl terminated polymers can be used as flexibilizers in epoxy resins.