212392-71-7

Basic information

• Product Name: N-(4-Chlorobenzyl)-4-fluorobenzylaMine, 97%
• Synonyms: N-(4-Chlorobenzyl)-4-fluorobenzylaMine, 97%;N-[(4-chlorophenyl)methyl]-1-(4-fluorophenyl)methanamine
• CAS NO: 212392-71-7
• Molecular Formula: C14H13ClFN
• Molecular Weight: 249.7111232
• Mol File: 212392-71-7.mol
• Article Data: 2

Chemical Properties

• Appearance: /
• CAS DataBase Reference: N-(4-Chlorobenzyl)-4-fluorobenzylaMine, 97%(CAS DataBase Reference)
• NIST Chemistry Reference: N-(4-Chlorobenzyl)-4-fluorobenzylaMine, 97%(212392-71-7)
• EPA Substance Registry System: N-(4-Chlorobenzyl)-4-fluorobenzylaMine, 97%(212392-71-7)

Safety Data

• Hazardous Substances Data: 212392-71-7(Hazardous Substances Data)

Upstream product

• 623-03-0 4-Cyanochlorobenzene 
• 140-75-0 para-fluorobenzylamine 
• 459-56-3 4-fluorobenzylic alcohol 
• 459-57-4 4-fluorobenzaldehyde 
• 104-86-9 4-chlorobenzylamine 

Relevant articles and documents

Switching Selectivity in Copper-Catalyzed Transfer Hydrogenation of Nitriles to Primary Amine-Boranes and Secondary Amines under Mild Conditions

A simple and efficient copper-catalyzed selective transfer hydrogenation of nitriles to primary amine-boranes and secondary amines with an oxazaborolidine-BH3 complex is reported. The selectivity control was achieved under mild conditions by switching the solvent and the copper catalysts. More than 30 primary amine-boranes and 40 secondary amines were synthesized via this strategy in high selectivity and yields of up to 95%. The strategy was applied to the synthesis of 15N labeled in 89% yield.