3,4-Dimethylpyridazine

Base Information

Chemical Name:3,4-Dimethylpyridazine
CAS No.:68206-10-0
Molecular Formula:C6H8 N2
Molecular Weight:108.143
Hs Code.:
European Community (EC) Number:888-055-4
DSSTox Substance ID:DTXSID80498340
Nikkaji Number:J1.002.415C
Wikidata:Q82348337

Synonyms:3,4-DIMETHYLPYRIDAZINE;68206-10-0;Pyridazine,3,4-dimethyl-;dimethyldiazine;SCHEMBL353403;SCHEMBL19919481;DTXSID80498340;EN300-221912;A836047

Suppliers and Price of 3,4-Dimethylpyridazine

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 7 raw suppliers

Chemical Property of 3,4-Dimethylpyridazine

Chemical Property:

XLogP3:0.6
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:0
Exact Mass:108.068748264
Heavy Atom Count:8
Complexity:72.9

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

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC1=C(N=NC=C1)C

Technology Process of 3,4-Dimethylpyridazine

There total 4 articles about 3,4-Dimethylpyridazine 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: 50.0%

: 289-80-5
1,2-diazine

: 64-19-7,77671-22-8
acetic acid

: 1120-88-3
4-methylpyridazine

: 22863-58-7
3,5-dimethyl-pyridazine

: 68206-10-0
3,4-dimethylpyridazine

: 38283-35-1
4,5-dimethylpyridazine

: 22868-72-0
3,4,5,6-tetramethylpyridazine

: 22863-59-8
3,4,5-trimethyl-pyridazine

Guidance literature:: With ammonium peroxydisulfate; silver nitrate; In sulfuric acid; at 90 ℃; for 1h; Product distribution; other 1,2-diazines, other source of methyl radical;