7-(Methanesulfonyl)-1-phenyl-1H-imidazo[4,5-d]pyridazine

Base Information

Chemical Name:7-(Methanesulfonyl)-1-phenyl-1H-imidazo[4,5-d]pyridazine
CAS No.:121433-41-8
Molecular Formula:C12H10N4O2S
Molecular Weight:274.303
Hs Code.:
DSSTox Substance ID:DTXSID30558600
Wikidata:Q82440963

Synonyms:121433-41-8;7-(Methylsulfonyl)-1-phenyl-1H-imidazo[4,5-d]pyridazine;7-(Methanesulfonyl)-1-phenyl-1H-imidazo[4,5-d]pyridazine;DTXSID30558600

Suppliers and Price of 7-(Methanesulfonyl)-1-phenyl-1H-imidazo[4,5-d]pyridazine

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
Packaging
price

Total 1 raw suppliers

Chemical Property of 7-(Methanesulfonyl)-1-phenyl-1H-imidazo[4,5-d]pyridazine

Chemical Property:

XLogP3:0.6
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:5
Rotatable Bond Count:2
Exact Mass:274.05244675
Heavy Atom Count:19
Complexity:416

Purity/Quality:: 99% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CS(=O)(=O)C1=C2C(=CN=N1)N=CN2C3=CC=CC=C3

Technology Process of 7-(Methanesulfonyl)-1-phenyl-1H-imidazo[4,5-d]pyridazine

There total 3 articles about 7-(Methanesulfonyl)-1-phenyl-1H-imidazo[4,5-d]pyridazine 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: 71.0%

: 121433-44-1
7-(methylthio)-1-phenyl-1H-imidazo<4,5-d>pyridazine

: 121433-41-8
7-(methylsulfonyl)-1-phenyl-1H-imidazo<4,5-d>pyridazine

Guidance literature:: With potassium permanganate; In acetic acid;
DOI:10.1248/cpb.37.13

Reference yield:

: 121433-42-9
7-chloro-1-phenyl-1H-imidazo<4,5-d>pyridazine

: 121433-41-8
7-(methylsulfonyl)-1-phenyl-1H-imidazo<4,5-d>pyridazine

Guidance literature:: Multi-step reaction with 3 steps

1: 77 percent / thiourea / ethanol / 1 h / Heating

2: 73 percent / 2N KOH / 0.17 h / Ambient temperature

3: 71 percent / 3percent KMnO₄ / acetic acid

With potassium hydroxide; potassium permanganate; thiourea; In ethanol; acetic acid;
DOI:10.1248/cpb.37.13

Reference yield:

: 121433-43-0
1-phenyl-1H-imidazo<4,5-d>pyridazine-7(6H)-thione

: 121433-41-8
7-(methylsulfonyl)-1-phenyl-1H-imidazo<4,5-d>pyridazine

Guidance literature:: Multi-step reaction with 2 steps

1: 73 percent / 2N KOH / 0.17 h / Ambient temperature

2: 71 percent / 3percent KMnO₄ / acetic acid

With potassium hydroxide; potassium permanganate; In acetic acid;
DOI:10.1248/cpb.37.13