(5-Aminopyridazin-4-yl)(2-fluorophenyl)methanone

Base Information

Chemical Name:(5-Aminopyridazin-4-yl)(2-fluorophenyl)methanone
CAS No.:96054-49-8
Molecular Formula:C11H8FN3O
Molecular Weight:217.202
Hs Code.:
DSSTox Substance ID:DTXSID60539649
Wikidata:Q82415438

Synonyms:96054-49-8;(5-Aminopyridazin-4-yl)(2-fluorophenyl)methanone;DTXSID60539649;(5-aminopyridazin-4-yl)-(2-fluorophenyl)methanone

Suppliers and Price of (5-Aminopyridazin-4-yl)(2-fluorophenyl)methanone

Supply Marketing:

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

Manufacturers and distributors:

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Total 0 raw suppliers

Chemical Property of (5-Aminopyridazin-4-yl)(2-fluorophenyl)methanone

Chemical Property:

XLogP3:1.2
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:5
Rotatable Bond Count:2
Exact Mass:217.06514005
Heavy Atom Count:16
Complexity:262

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC=C(C(=C1)C(=O)C2=CN=NC=C2N)F

Technology Process of (5-Aminopyridazin-4-yl)(2-fluorophenyl)methanone

There total 2 articles about (5-Aminopyridazin-4-yl)(2-fluorophenyl)methanone 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:

: 96087-97-7
7-Chlor-7-(2-fluorphenyl)furo<3,4-d>pyridazin-5(7H)-on

: 96054-49-8
5-aminopyridazin-4-yl o-fluorophenyl ketone

Guidance literature:: Multi-step reaction with 2 steps

1: aq. NaN₃ / acetone / 1) 15 min, ice cooling, 2) 1 h, room temperature

2: 91 mg / benzene / 4 h / Heating

With sodium azide; In acetone; benzene;

Reference yield:

: 86839-78-3
5-(2-Fluorobenzoyl)-4-pyridazinecarboxylic Acid

: 96054-49-8
5-aminopyridazin-4-yl o-fluorophenyl ketone

Guidance literature:: Multi-step reaction with 3 steps

1: 95 percent / thionyl chloride / 4 h / Heating

2: aq. NaN₃ / acetone / 1) 15 min, ice cooling, 2) 1 h, room temperature

3: 91 mg / benzene / 4 h / Heating

With thionyl chloride; sodium azide; In acetone; benzene;