34243-68-0

Basic information

• Product Name: 1-phenylmethanamine benzoate (1:1)
• CAS NO: 34243-68-0
• Molecular Formula: C₇H₆O₂*C₇H₉N
• Molecular Weight: 229.2744
• Mol File: 34243-68-0.mol
• Article Data: 4

Chemical Properties

• Boiling Point: 249.3°C at 760 mmHg
• Flash Point: 111.4°C
• Vapor Pressure: 0.0122mmHg at 25°C
• CAS DataBase Reference: 1-phenylmethanamine benzoate (1:1)(CAS DataBase Reference)
• NIST Chemistry Reference: 1-phenylmethanamine benzoate (1:1)(34243-68-0)
• EPA Substance Registry System: 1-phenylmethanamine benzoate (1:1)(34243-68-0)

Safety Data

• Hazardous Substances Data: 34243-68-0(Hazardous Substances Data)

Usage

Usage

Commonly used in the pharmaceutical industry as an intermediate in the synthesis of various drugs.

Molecular weight

215.24 g/mol.

Appearance

White to off-white crystalline powder.

Solubility

Soluble in organic solvents such as methanol and ethanol.

Primary use

As a reagent in organic synthesis and as a pharmaceutical intermediate for the production of various medications.

Upstream product

• 134-81-6 benzil 
• 100-46-9 benzylamine 
• 119-53-9 2-hydroxy-2-phenylacetophenone 
• 65-85-0 benzoic acid 
• 1750-74-9 2-benzoyl-2-methylpropanal 
• 64-17-5 ethanol 
• 94-36-0 dibenzoyl peroxide 
• 105361-41-9 N-benzyl-2-benzoyl-2-methylpropanimine 

Downstream Products

• 1485-70-7 N-benzylbenzamide 

Relevant articles and documents

Electrogenerated superoxide anion induced oxidative amidation of benzoin

Amide function is very important in both organic and medicinal chemistry. Benzamides can be obtained in good to high yields by reaction of benzoin, primary or secondary amines, molecular oxygen and electrogenerated superoxide anion (obtained with galvanos

Benzoic acid-catalyzed transamidation reactions of carboxamides, phthalimide, ureas and thioamide with amines

An efficient and simple method for the transamidation of carboxamides, phthalimide, ureas and thioamide with amines catalyzed by commercially available benzoic acid under metal-free conditions is described. Furthermore, to the best of our knowledge, this is the first report about the transamidation of an aromatic thioamide with amines.