405551-69-1

Basic information

• Product Name: 3-(4-chloro-phenyl)-3-pyridin-2-yl-acrylonitrile
• Synonyms: 3-(4-chloro-phenyl)-3-pyridin-2-yl-acrylonitrile
• CAS NO: 405551-69-1
• Molecular Weight: 240.692
• Mol File: 405551-69-1.mol

Chemical Properties

• CAS DataBase Reference: 3-(4-chloro-phenyl)-3-pyridin-2-yl-acrylonitrile(CAS DataBase Reference)
• NIST Chemistry Reference: 3-(4-chloro-phenyl)-3-pyridin-2-yl-acrylonitrile(405551-69-1)
• EPA Substance Registry System: 3-(4-chloro-phenyl)-3-pyridin-2-yl-acrylonitrile(405551-69-1)

Safety Data

• Hazardous Substances Data: 405551-69-1(Hazardous Substances Data)

Upstream product

• 6318-51-0 2-(4-chlorobenzoyl)pyridine 
• 15898-47-2 (cyanomethyl)triphenylphosphonium bromide 
• 160911-84-2 1-(4-chlorophenyl-1-(2-pyridyl))ehylene 

Downstream Products

• 405551-87-3 1-[3-(4-chloro-phenyl)-3-pyridin-2-yl-propyl]-3-[4-(1-trityl-1H-imidazol-4-yl)-butyl]-urea 
• 405551-76-0 N-[3-(4-chloro-phenyl)-3-pyridin-2-yl-propyl]-4-(1-trityl-1H-imidazol-4-yl)-butyramidine 
• 405551-81-7 N-[3-(4-chloro-phenyl)-3-pyridin-2-yl-propyl]-N-methyl-3-(1-trityl-1H-imidazol-4-yl)-propionamide 
• 405551-80-6 N-[3-(4-chloro-phenyl)-3-pyridin-2-yl-propyl]-3-(1-trityl-1H-imidazol-4-yl)-propionamide 
• 725738-26-1 [3-(4-chloro-phenyl)-3-pyridin-2-yl-propyl]-[3-(1-trityl-1H-imidazol-4-yl)-propyl]-amine 
• 725738-46-5 [3-(4-chloro-phenyl)-3-pyridin-2-yl-propyl]-methyl-[3-(1-trityl-1H-imidazol-4-yl)-propyl]-amine 
• 405551-74-8 2-[1-(4-chloro-phenyl)-3-isocyanato-propyl]-pyridine 
• 20619-13-0 Didesmethylchlorpheniramine 
• 405551-70-4 3-(4-chlorophenyl)-3-(pyridin-2-yl)propanenitrile 

Relevant articles and documents

Copper-Catalyzed C-H Stereoselective Cyanation of Alkenes by Using an α-Iminonitrile as a Cyanating Reagent

The first copper-catalyzed cyanation through alkene C-H bond activation by using an α-iminonitrile as a cyanating agent has been realized. The approach efficiently constructs acrylonitriles in good yields with the advantages of high regioselectivity, cost

Identification of a dual histamine H1/H3 receptor ligand based on the H1 antagonist chlorpheniramine

Combining the first generation H1 antihistamine chlorpheniramine (1) with H3 ligands of the alkylamine type has led to the identification of compound 9d, a dual ligand of both the H1 and H3 receptors.