4-Amino-phenyl-3-chloropyridazine

Base Information

Chemical Name:4-Amino-phenyl-3-chloropyridazine
CAS No.:108655-24-9
Molecular Formula:C₁₀H₈ClN₃
Molecular Weight:205.647
Hs Code.:
DSSTox Substance ID:DTXSID001287259

Synonyms:4-amino-phenyl-3-chloropyridazine;108655-24-9;DTXSID001287259;4-(3-Chloro-4-pyridazinyl)benzenamine

Suppliers and Price of 4-Amino-phenyl-3-chloropyridazine

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
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price

Total 1 raw suppliers

Chemical Property of 4-Amino-phenyl-3-chloropyridazine

Chemical Property:

XLogP3:1.8
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:1
Exact Mass:205.0406750
Heavy Atom Count:14
Complexity:180

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:C1=CC(=CC=C1C2=C(N=NC=C2)Cl)N

Technology Process of 4-Amino-phenyl-3-chloropyridazine

There total 2 articles about 4-Amino-phenyl-3-chloropyridazine which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 16.0%

: 29512-30-9
4-(p-Nitrophenyl)-3,6-dichloropyridazine

: 108655-23-8
4-(p-aminophenyl)pyridazine

: 108655-24-9
4-(p-Aminophenyl)-3-chloropyridazine

: 29512-31-0
4-(p-Aminophenyl)-3,6-dichloropyridazine

Guidance literature:: With hydrogen; sodium acetate; acetic acid; palladium on activated charcoal; In ethanol; at 40 ℃;
DOI:10.1007/BF00522738

Reference yield:

: 29512-29-6
4-(p-Nitrophenyl)-3,6-dioxo-1,2,3,6-tetrahydropyridazine

: 108655-24-9
4-(p-Aminophenyl)-3-chloropyridazine

Guidance literature:: Multi-step reaction with 2 steps

1: POCl₃ / 1 h / Heating

2: 22 percent / sodium acetate, hydrogen, acetic acid / 10percent palladium on carbon / ethanol / 40 °C

With hydrogen; sodium acetate; acetic acid; trichlorophosphate; palladium on activated charcoal; In ethanol;
DOI:10.1007/BF00522738