21103-30-0

Basic information

• Product Name: 2-[4-(3-chlorophenyl)-1-piperazinyl]ethylamine
• Synonyms: 2-[4-(3-chlorophenyl)-1-piperazinyl]ethylamine
• CAS NO: 21103-30-0
• Molecular Weight: 239.748
• Mol File: 21103-30-0.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: 2-[4-(3-chlorophenyl)-1-piperazinyl]ethylamine(CAS DataBase Reference)
• NIST Chemistry Reference: 2-[4-(3-chlorophenyl)-1-piperazinyl]ethylamine(21103-30-0)
• EPA Substance Registry System: 2-[4-(3-chlorophenyl)-1-piperazinyl]ethylamine(21103-30-0)

Safety Data

• Hazardous Substances Data: 21103-30-0(Hazardous Substances Data)

Upstream product

• 6640-24-0 N-(m-chlorophenyl)piperazine 
• 75000-29-2 2-(2-(4-(3-chlorophenyl)piperazin-1-yl)ethyl)isoindoline-1,3-dione 

Downstream Products

• 1146214-46-1 N-[2-{4-(3-chlorophenyl)-piperazin-1-yl}-ethyl]-pyrrolidine-2,5-dione 
• 1146214-48-3 N-[2-{4-(3-chlorophenyl)-piperazin-1-yl}-ethyl]-3-cyclohexyl-pyrrolidine-2,5-dione 
• 1240266-51-6 C₂₅H₃₁ClN₄O*ClH 
• 1262099-35-3 C₂₃H₂₆ClN₃O₂ 
• 1221290-68-1 N-{2-[4-(3-chlorophenyl)piperazin-1-yl]ethyl}-2-quinoxaline carboxamide 
• 1221290-90-9 N-{2-[4-(3-chlorophenyl)piperazin-1-yl]ethyl}-3-quinoline carboxamide 
• 1221290-78-3 N-{2-[4-(3-chlorophenyl)piperazin-1-yl]ethyl}-2-quinoline carboxamide 
• 1155401-85-6 N-[2-{4-(3-chlorophenyl)-piperazin-1-yl}-ethyl]-3-(2-methylphenyl)-pyrrolidine-2,5-dione hydrochloride 
• 1155401-94-7 N-[2-{4-(3-chlorophenyl)-piperazin-1-yl}-ethyl]-3-(2-trifluoromethylphenyl)-pyrrolidine-2,5-dione hydrochloride 
• 184691-44-9 2-{2-[4-(3-Chloro-phenyl)-piperazin-1-yl]-ethyl}-9-methyl-4,9-dihydro-β-carboline-1,3-dione 
• 184691-41-6 2-{2-[4-(3-Chloro-phenyl)-piperazin-1-yl]-ethyl}-4,9-dihydro-β-carboline-1,3-dione 

Relevant articles and documents

Small-Molecule Inhibition of the UNC119–Cargo Interaction

N-Terminal myristoylation facilitates membrane binding and activity of proteins, in particular of Src family kinases, but the underlying mechanisms are only beginning to be understood. The chaperones UNC119A/B regulate the cellular distribution and signal

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T-type calcium channel is one of therapeutic targets for the treatment of cardiovascular diseases and neuropathic pain. In this study, as a part of our ongoing efforts to develop potent T-type calcium channel blockers, we designed oxazole derivatives subs

Synthesis and pharmacology of 1-(4-aryl-1-piperazinyl-alkyl)-4-(4-methoxyphenyl) piperidine-2,6-diones: Tranquilizers

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