496035-25-7

Basic information

• Product Name: Benzenamine, N-[(4-chlorophenyl)methylene]-3-(1,3,2-dioxaborinan-2-yl)-
• CAS NO: 496035-25-7
• Molecular Formula: C16H15BClNO2
• Molecular Weight: 299.565
• Mol File: 496035-25-7.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: Benzenamine, N-[(4-chlorophenyl)methylene]-3-(1,3,2-dioxaborinan-2-yl)-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzenamine, N-[(4-chlorophenyl)methylene]-3-(1,3,2-dioxaborinan-2-yl)-(496035-25-7)
• EPA Substance Registry System: Benzenamine, N-[(4-chlorophenyl)methylene]-3-(1,3,2-dioxaborinan-2-yl)-(496035-25-7)

Safety Data

• Hazardous Substances Data: 496035-25-7(Hazardous Substances Data)

Upstream product

• 30418-59-8 3-Aminophenylboronic acid 
• 104-88-1 4-chlorobenzaldehyde 
• 210775-52-3 3-[1,3,2]dioxaborinan-2-yl-phenylamine 

Relevant articles and documents

Saccharide-accelerated hydrolysis of boronic acid imines

Twenty substituted N-benzylidineaniline derivatives have been synthesised and their kinetic behaviour investigated. The rate of hydrolysis of the boronic acid imines was found to be accelerated by added saccharide. Catalytic activity was only observed below the pKa of the boronic acid. Altering the concentration or type of saccharide revealed a Bronsted-like linear free energy relationship, indicating that intramolecular general acid catalysis was operating. Structure-activity relationship studies demonstrated that the system's electronic demands were independent of the boronic acid moiety.