5096-76-4

Basic information

• Product Name: 3-CHLORO-6-PYRROL-1-YL-PYRIDAZINE
• Synonyms: 3-CHLORO-6-PYRROL-1-YL-PYRIDAZINE;3-Chloro-6-(1H-pyrrol-1-yl)pyridazine 98%;3-Chloro-6-(1H-pyrrol-1-yl)pyridazine;Zinc02570319;3-Chloro-6-(1H-pyrrol-1-yl)pyridazine98%
• CAS NO: 5096-76-4
• Molecular Formula: C₈H₆ClN₃
• Molecular Weight: 179.61
• Product Categories: blocks;Imidazoles;Pyridines
• Mol File: 5096-76-4.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 357.6 °C at 760 mmHg
• Flash Point: 170.1 °C
• Appearance: /
• Density: 1.34 g/cm³
• Vapor Pressure: 5.55E-05mmHg at 25°C
• Refractive Index: 1.653
• CAS DataBase Reference: 3-CHLORO-6-PYRROL-1-YL-PYRIDAZINE(CAS DataBase Reference)
• NIST Chemistry Reference: 3-CHLORO-6-PYRROL-1-YL-PYRIDAZINE(5096-76-4)
• EPA Substance Registry System: 3-CHLORO-6-PYRROL-1-YL-PYRIDAZINE(5096-76-4)

Safety Data

• Hazard Codes: Xi
• Hazardous Substances Data: 5096-76-4(Hazardous Substances Data)

Usage

General Description

3-Chloro-6-pyrrol-1-yl-pyridazine is a chemical compound with the molecular formula C9H6ClN3. It is a pyridazine derivative with a chlorine atom and a pyrrole ring attached to the pyridazine ring. 3-Chloro-6-pyrrol-1-yl-pyridazine has potential applications in pharmaceuticals, agrochemicals, and materials science due to its unique chemical structure and reactivity. It may also have biological activity and could be used as a building block in organic synthesis. Further research and development of this compound could lead to its use in various industrial and scientific applications.

InChI:InChI=1/C8H6ClN3/c9-7-3-4-8(11-10-7)12-5-1-2-6-12/h1-6H

Upstream product

• 696-59-3 cis,trans-2,5-dimethoxytetrahydrofuran 
• 5469-69-2 6-chloro-pyridazin-3-ylamine 
• 141-30-0 3,6-dichlorpyridazine 
• 109-97-7 pyrrole 

Downstream Products

• 1417455-19-6 methyl 3-[6-(1H-pyrrol-1-yl)pyridazin-3-yl]benzoate 
• 138803-58-4 1-[2-(2-Methoxy-phenoxy)-ethylamino]-3-(6-pyrrol-1-yl-pyridazin-3-yloxy)-propan-2-ol 
• 138803-59-5 1-[2-(4-Fluoro-phenoxy)-ethylamino]-3-(6-pyrrol-1-yl-pyridazin-3-yloxy)-propan-2-ol 
• 138803-57-3 1-(2-Phenoxy-ethylamino)-3-(6-pyrrol-1-yl-pyridazin-3-yloxy)-propan-2-ol 

Relevant articles and documents

Selective mono-amination of dichlorodiazines

A mild, easy-to-perform, and versatile method for the formation of aminochlorodiazines from reaction of several types of dichlorodiazines (i.e., pyridazines, pyrimidines, and pyrazines) with primary or secondary amines in ethanol in the presence of trieth

Synthesis and antihypertensive activity of new 6-heteroaryl-3-hydrazinopyridazine derivatives

The synthesis and pharmacological activity of new 6-heteroaryl-3-hydrazinopyridazines with antihypertensive action are described. The introduction of pyrrole, pyrazole, imidazole, triazole, tetrazole, thiophene, indole, and carbazole heterocyclic rings into the 6 position of the pyridazine nucleus has been carried out by three different methods of synthesis. The hypotensive action has been examined on normotensive and spontaneously hypertensive rats by comparison with dihydralazine (I). 6-Imidazol-1-yl derivatives have proved particularly active. Of these derivatives 3-hydrazino-6-(2-methylimidazol-1-yl)pyridazine (7c) achieves 4.9 times the activity of dihydralazine when administered orally to spontaneously hypertensive rats. The LD50 values of 7c and dihydralazine are very similar.