126541-65-9

Basic information

• Product Name: N-(benzotriazol-1-yl-methyl)-cyclohexylamine
• Synonyms: N-(benzotriazol-1-yl-methyl)-cyclohexylamine
• CAS NO: 126541-65-9
• Molecular Weight: 230.313
• Mol File: 126541-65-9.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: N-(benzotriazol-1-yl-methyl)-cyclohexylamine(CAS DataBase Reference)
• NIST Chemistry Reference: N-(benzotriazol-1-yl-methyl)-cyclohexylamine(126541-65-9)
• EPA Substance Registry System: N-(benzotriazol-1-yl-methyl)-cyclohexylamine(126541-65-9)

Safety Data

• Hazardous Substances Data: 126541-65-9(Hazardous Substances Data)

Upstream product

• 95-14-7 1,2,3-Benzotriazole 
• 50-00-0 formaldehyd 
• 108-91-8 cyclohexylamine 

Downstream Products

• 1137869-48-7 3-cyclohexylamino-2,2-difluoropropionic acid ethyl ester 
• 100051-14-7 cyclohexyl-pyrrol-2-ylmethyl-amine 
• 142920-58-9 Cyclohexyl-(1-methyl-1H-pyrrol-2-ylmethyl)-amine 
• 126541-72-8 N-cyclohexyl-2-phenylethylamine hydrochloride 
• 16350-96-2 N-cyclohexyl-benzenemethanamine hydrochloride 
• 1074-58-4 N-(cyanomethyl)cyclohexylamine 
• 130564-38-4 Cyclohexyl-(1-nitro-cyclohexylmethyl)-amine 
• 73825-68-0 cyclohexyl-(β-nitro-isobutyl)-amine 
• 3592-82-3 N-propylcyclohexylamine hydrochloride 
• 53924-03-1 N-indol-3-ylmethylcyclohexylamine 
• 142920-60-3 Cyclohexyl-(1-methyl-1H-indol-3-ylmethyl)-amine 

Relevant articles and documents

aminoalkylbenzotriazoles: Reagents for the aminoalkylation of electron rich heterocycles

Secondary and tertiary aminoalkylbenzotriazoles react with pyrrole, indole, their N-methyl analogs and with 2-methylfuran under mild reaction conditions in the presence of a Lewis acid to afford selectively the corresponding secondary or tertiary amines.

The N-Substitution of Aliphatic Primary Amines via 1-benzotriazoles: Preparation of Secondary Amines

A new method has been developed for the selective conversion of primary aliphatic amines into unsymmetrical secondary amines by Grignard reaction of 1-benzotriazoles 1.This method employs simple procedures and mild conditions, and is specific in that onyl monoalkylation of the primary amines results.