927801-09-0

Basic information

• Product Name: 3-BROMO-7-CHLORO-4-(PIPERAZIN-1-YL)QUINOLINE
• Synonyms: 3-Bromo-7-chloro-4-(piperazin-1-yl)quinoline; quinoline, 3-bromo-7-chloro-4-(1-piperazinyl)-
• CAS NO: 927801-09-0
• Molecular Formula: C13H13 Br Cl N3
• Molecular Weight: 326.62
• Mol File: 927801-09-0.mol
• Article Data: 0

Chemical Properties

• Boiling Point: 458.1°C at 760 mmHg
• Flash Point: 230.8°C
• Appearance: /
• Density: 1.531g/cm³
• Vapor Pressure: 1.42E-08mmHg at 25°C
• Refractive Index: 1.655
• Storage Temp.: 2-8°C
• CAS DataBase Reference: 3-BROMO-7-CHLORO-4-(PIPERAZIN-1-YL)QUINOLINE(CAS DataBase Reference)
• NIST Chemistry Reference: 3-BROMO-7-CHLORO-4-(PIPERAZIN-1-YL)QUINOLINE(927801-09-0)
• EPA Substance Registry System: 3-BROMO-7-CHLORO-4-(PIPERAZIN-1-YL)QUINOLINE(927801-09-0)

Safety Data

• Hazardous Substances Data: 927801-09-0(Hazardous Substances Data)

Usage

Description

3-Bromo-7-chloro-4-(piperazin-1-yl)quinoline is a heterocyclic organic compound that belongs to the quinoline family. It features a quinoline backbone with bromine and chlorine substituents at the 3 and 7 positions, respectively, and a piperazine ring attached to the 4 position. This chemical structure endows it with potential applications in medicinal chemistry, particularly for the development of new drugs.

Uses

Used in Medicinal Chemistry:
3-Bromo-7-chloro-4-(piperazin-1-yl)quinoline is used as a chemical intermediate for the development of new drugs due to its unique structure and properties.
Used in Antimicrobial Applications:
In the pharmaceutical industry, 3-Bromo-7-chloro-4-(piperazin-1-yl)quinoline is used as an antimicrobial agent for its ability to inhibit the growth and reproduction of certain microorganisms.
Used in Antiparasitic Applications:
3-Bromo-7-chloro-4-(piperazin-1-yl)quinoline is used as an antiparasitic agent, leveraging its capacity to curb the proliferation of specific parasites.
Used in Anti-cancer Applications:
3-Bromo-7-chloro-4-(piperazin-1-yl)quinoline is used as a potential anti-cancer agent, being investigated for its possible role in combating cancer cells.
Overall, the chemical structure of 3-Bromo-7-chloro-4-(piperazin-1-yl)quinoline makes it a versatile compound with potential applications in various fields of research, particularly in the development of pharmaceuticals for infectious diseases and cancer treatment.

InChI:InChI=1/C13H13BrClN3/c14-11-8-17-12-7-9(15)1-2-10(12)13(11)18-5-3-16-4-6-18/h1-2,7-8,16H,3-6H2