186650-78-2

Basic information

• Product Name: 4-(4-ethyl-piperazin-1-yl)-benzonitrile
• Synonyms: 4-(4-ethyl-piperazin-1-yl)-benzonitrile
• CAS NO: 186650-78-2
• Molecular Weight: 215.298
• Mol File: 186650-78-2.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: 4-(4-ethyl-piperazin-1-yl)-benzonitrile(CAS DataBase Reference)
• NIST Chemistry Reference: 4-(4-ethyl-piperazin-1-yl)-benzonitrile(186650-78-2)
• EPA Substance Registry System: 4-(4-ethyl-piperazin-1-yl)-benzonitrile(186650-78-2)

Safety Data

• Hazardous Substances Data: 186650-78-2(Hazardous Substances Data)

Upstream product

• 75-07-0 acetaldehyde 
• 68104-63-2 N-(4-cyanophenyl)piperazine 
• 5308-25-8 4-ethylpiperazine 
• 623-00-7 4-bromobenzenecarbonitrile 
• 75-03-6 ethyl iodide 

Downstream Products

• 402745-30-6 [4-(4-ethylpiperazinyl)phenyl]methan-1-ol 
• 179328-89-3 N,N'-Diethyl-N-[4-(4-ethyl-piperazin-1-yl)-benzyl]-ethane-1,2-diamine 
• 197638-69-0 N'-Ethyl-N-[4-(4-ethyl-piperazin-1-yl)-benzyl]-N-methyl-ethane-1,2-diamine 
• 197638-81-6 (2-Chloro-ethyl)-[4-(4-ethyl-piperazin-1-yl)-benzyl]-methyl-amine 
• 197638-79-2 [4-(4-Ethyl-piperazin-1-yl)-benzyl]-methyl-amine 
• 197638-76-9 4-(4-ethylpiperazin-1-yl)benzaldehyde 

Relevant articles and documents

USE OF DISUBSTITUTED BENZENES TO CONTROL INSECTICIDE-RESISTANT PESTS

The invention is in the technical field of insect control and relates to the use of a disubstituted benzenes for controlling insecticide-resistant pests such as mosquitoes and cockroaches.

Dissection of N,N-diethyl-N′-phenylpiperazines as α7 nicotinic receptor silent agonists This manuscript is dedicated to Professor Koji Nakanishi on the occasion of his 90th birthday

The α7 nicotinic acetylcholine receptor (nAChR) is a target for control of inflammation-related phenomena via compounds that are able to selectively induce desensitized states of the receptor. Compounds that selectively desensitize, without facilitating s

An efficient, palladium-catalysed, amination of aryl bromides

Aryl bromides are coupled to primary aliphatic amines, anilines and cyclic secondary amines in an efficient and selective procedure using catalytic amounts of Pd(OAc)2 and the chelating ligand 9,9-dimethyl- 4,6bis(diphenylphosphino)xanthene (Xa