52536-36-4

Basic information

• Product Name: 1-(2-chlorophenyl)-4-(3-chloropropyl)piperazine
• CAS NO: 52536-36-4
• Molecular Formula: C₁₃H₁₈Cl₂N₂
• Molecular Weight: 273.2014
• Mol File: 52536-36-4.mol
• Article Data: 5

Chemical Properties

• Boiling Point: 380.7°C at 760 mmHg
• Flash Point: 184°C
• Density: 1.186g/cm³
• Vapor Pressure: 5.36E-06mmHg at 25°C
• Refractive Index: 1.553
• CAS DataBase Reference: 1-(2-chlorophenyl)-4-(3-chloropropyl)piperazine(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(2-chlorophenyl)-4-(3-chloropropyl)piperazine(52536-36-4)
• EPA Substance Registry System: 1-(2-chlorophenyl)-4-(3-chloropropyl)piperazine(52536-36-4)

Safety Data

• Hazardous Substances Data: 52536-36-4(Hazardous Substances Data)

Usage

Description

1-(2-chlorophenyl)-4-(3-chloropropyl)piperazine, also known as 2C-C-NBOMe, is a chemical compound belonging to the phenethylamine class and featuring a piperazine side chain. It is a derivative of the psychedelic drug 2C-C and is part of the NBOMe family of hallucinogenic substances. 1-(2-chlorophenyl)-4-(3-chloropropyl)piperazine is known for its potent hallucinogenic effects, which include visual and auditory distortions, altered thinking and sense of time, and changes in perception and mood.

Uses

Used in Scientific Research:
1-(2-chlorophenyl)-4-(3-chloropropyl)piperazine is used as a research chemical for the study of its hallucinogenic properties and potential interactions with the human brain. It provides valuable insights into the mechanisms of action of psychedelic substances and their effects on cognitive and perceptual processes.

Upstream product

• 39512-50-0 N-(o-Chlorophenyl)piperazine 
• 109-70-6 1.3-chlorobromopropane 

Downstream Products

• 114694-59-6 1-[4-(2-chloro-phenyl)-piperazino]-3-(4-m-tolyl-piperazino)-propane 
• 114694-61-0 1-[4-(2-chloro-phenyl)-piperazino]-3-(4-p-tolyl-piperazino)-propane 
• 114694-60-9 1-[4-(2-chloro-phenyl)-piperazino]-3-(4-o-tolyl-piperazino)-propane 
• 6323-10-0 1-[4-(2-chloro-phenyl)-piperazino]-3-[4-(3-chloro-phenyl)-piperazino]-propane 
• 115098-04-9 1-[4-(2-chloro-phenyl)-piperazino]-3-[4-(4-chloro-phenyl)-piperazino]-propane 
• 91532-35-3 3-{3-[4-(2-Chloro-phenyl)-piperazin-1-yl]-propyl}-3H-benzo[d][1,2,3]triazin-4-one 
• 84344-60-5 1-(2-Chloro-phenyl)-4-[3-(2-nitro-phenoxy)-propyl]-piperazine 
• 174519-56-3 N¹-{3-[4-(2-Chloro-phenyl)-piperazin-1-yl]-propyl}-ethane-1,2-diamine 

Relevant articles and documents

Regioselective click chemistry for construction of arylpiperazinyl 1,2,3-triazole derivative libraries as dopamine D4/D3 receptor ligands

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Synthesis of new 1-[3-(4-phenylpiperazinyl-1)propyl[-imidazolidine derivatives

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Synthesis and Biological Activities of 3-Substituted 1-Aryloxyaminopropanes

A number of 3-substituted 1-aryloxyaminopropanes (9-43) have been prepared by the reaction of appropriate hydroxyaryl compound with 1-chloro-3-1-(N4-aryl-piperazinyl/piperidinyl)>propanes (1-8).The 1-(6/7-quinolyloxy)-3-substituted