62167-06-0

Basic information

• Product Name: Benzenamine, 2-[(4-chlorophenyl)ethynyl]-N,N-dimethyl-
• CAS NO: 62167-06-0
• Molecular Formula: C16H14ClN
• Molecular Weight: 255.747
• Mol File: 62167-06-0.mol

Chemical Properties

• CAS DataBase Reference: Benzenamine, 2-[(4-chlorophenyl)ethynyl]-N,N-dimethyl-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzenamine, 2-[(4-chlorophenyl)ethynyl]-N,N-dimethyl-(62167-06-0)
• EPA Substance Registry System: Benzenamine, 2-[(4-chlorophenyl)ethynyl]-N,N-dimethyl-(62167-06-0)

Safety Data

• Hazardous Substances Data: 62167-06-0(Hazardous Substances Data)

Upstream product

• 873-73-4 4-n-chlorophenylacetylene 
• 698-02-2 N,N-dimethyl-o-iodoaniline 

Downstream Products

• 1401560-34-6 3-chloro-11-methyl-5,6-diphenyl-11H-benzo[a]carbazole 
• 1448145-38-7 2-(4-chlorophenyl)-N-methyl-3-(phenylselenyl)-1H-indole 
• 5905-11-3 2-(4-chlorophenyl)-1-methyl-2-phenyl-1H-indole 
• 1618087-09-4 11-(4-chlorophenyl)-5-methyl-6-phenyl-5H-indeno[1,2-c]quinoline 
• 1516898-80-8 C₁₆H₁₁ClF₃NS 
• 938326-81-9 2-(4-chlorophenyl)-1-methyl-1H-indole-3-carbonitrile 

Relevant articles and documents

CuBr-promoted tandem cyclization/trifluoromethylation of 2-alkynylanilines: Efficient synthesis of 3-trifluoromethylindoles

A new efficient strategy for the synthesis of 3-trifluoromethyl-indoles was developed through tandem cyclization/ trifluoromethylation of 2-alkynylanilines and Umemoto’s reagent under effect of CuBr. The reaction features the use of cheap copper salt, mil

Palladium(II)-catalyzed tandem cyclization/C-H functionalization of alkynes for the synthesis of functionalized indoles

A palladium-catalyzed tandem cyclization/C-H functionalization of two alkynes was accomplished to construct a series of polycyclic functionalized indoles. A range of internal alkynes bearing synthetically useful functional groups were tolerated. A good regioselectivity was observed when alkyl-substituted alkynes were introduced into the reaction system, and a single product was obtained. Molecular oxygen was used as the terminal oxidant in the approach, rendering the reaction more sustainable.