6323-15-5

Basic information

• Product Name: 1-(3-chloropropyl)-4-(2-methylphenyl)piperazine
• CAS NO: 6323-15-5
• Molecular Formula: C₁₄H₂₁ClN₂
• Molecular Weight: 252.7829
• Mol File: 6323-15-5.mol
• Article Data: 2

Chemical Properties

• Boiling Point: 368.2°C at 760 mmHg
• Flash Point: 176.5°C
• Density: 1.077g/cm³
• Vapor Pressure: 1.29E-05mmHg at 25°C
• Refractive Index: 1.54
• CAS DataBase Reference: 1-(3-chloropropyl)-4-(2-methylphenyl)piperazine(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(3-chloropropyl)-4-(2-methylphenyl)piperazine(6323-15-5)
• EPA Substance Registry System: 1-(3-chloropropyl)-4-(2-methylphenyl)piperazine(6323-15-5)

Safety Data

• Hazardous Substances Data: 6323-15-5(Hazardous Substances Data)

Usage

Description

1-(3-chloropropyl)-4-(2-methylphenyl)piperazine is a chemical compound featuring a piperazine ring with a 3-chloropropyl group and a 2-methylphenyl group attached to it. It is recognized for its potential biological activity and pharmacological properties, making it a compound of interest in the field of pharmaceuticals and organic chemistry. Due to its potential hazards and reactivity, it is crucial to handle this compound with caution and adhere to proper safety protocols.

Uses

Used in Pharmaceutical Synthesis:
1-(3-chloropropyl)-4-(2-methylphenyl)piperazine is used as an intermediate in the synthesis of various pharmaceuticals and organic compounds. Its unique structure and potential biological activity make it a valuable component in the development of new drugs and therapeutic agents.
Used in Research and Development:
In the field of research and development, 1-(3-chloropropyl)-4-(2-methylphenyl)piperazine is utilized for studying its pharmacological properties and potential applications in medicine. This includes exploring its interactions with biological systems and assessing its efficacy in treating specific conditions or diseases.
Used in Chemical Industry:
1-(3-chloropropyl)-4-(2-methylphenyl)piperazine is also employed in the chemical industry as a building block for the creation of other complex organic molecules. Its versatile structure allows for further functionalization and modification, making it a useful starting material for the synthesis of a wide range of compounds with various applications.

Upstream product

• 109-99-9 tetrahydrofuran 
• 39512-51-1 1-(o-toluyl)piperazine 
• 109-70-6 1.3-chlorobromopropane 

Downstream Products

• 1454854-95-5 C₂₂H₂₆FN₅ 
• 1454855-05-0 C₂₂H₂₆FN₅ 
• 326497-34-1 2-[3-(4-o-tolyl-piperazin-1-yl)-propyl]-tetrahydro-imidazo[1,5-a]pyridine-1,3-dione 
• 91532-36-4 3-[3-(4-o-Tolyl-piperazin-1-yl)-propyl]-3H-benzo[d][1,2,3]triazin-4-one 
• 114694-60-9 1-[4-(2-chloro-phenyl)-piperazino]-3-(4-o-tolyl-piperazino)-propane 
• 6320-27-0 1-[4-(4-chloro-phenyl)-piperazino]-3-(4-o-tolyl-piperazino)-propane 
• 114694-57-4 1-[4-(3-chloro-phenyl)-piperazino]-3-(4-o-tolyl-piperazino)-propane 
• 116030-53-6 1-(4-o-tolyl-piperazino)-3-(4-p-tolyl-piperazino)-propane 
• 116030-90-1 1-(4-m-tolyl-piperazino)-3-(4-o-tolyl-piperazino)-propane 
• 6323-13-3 1-(4-phenyl-piperazino)-3-(4-o-tolyl-piperazino)-propane 

Relevant articles and documents

N6 -Substituted-9-[3-(4-phenyl-piperazino)-propyl]-adenines

A N6 -substituted-9-[3-(4-phenyl-piperazino)-propyl]-adenine of the formula STR1 wherein R1 is hydrogen or a lower alkyl radical, and R2 is a lower alkyl radical, a lower alkyl radical substituted by at least one of phenyl