2-Methylquinoxaline 1,4-dioxide

Base Information

Chemical Name:2-Methylquinoxaline 1,4-dioxide
CAS No.:6639-86-7
Molecular Formula:C9H8 N2 O2
Molecular Weight:176.175
Hs Code.:2933990090
European Community (EC) Number:229-648-4
NSC Number:48949,47510,47509
DSSTox Substance ID:DTXSID10216615
Nikkaji Number:J298.030D
Wikidata:Q83092863
ChEMBL ID:CHEMBL1989025
Mol file:6639-86-7.mol

Synonyms:2-methylquinoxaline 1,4-dioxide;2-MQDO

Suppliers and Price of 2-Methylquinoxaline 1,4-dioxide

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

TRC
2-METHYLQUINOXALINE 1,4-DIOXIDE
250 mg
$ 350.00

Sigma-Aldrich
2-METHYLQUINOXALINE 1,4-DIOXIDE AldrichCPR
1ea
$ 144.00

American Custom Chemicals Corporation
2-METHYLQUINOXALINEDIIUM-1,4-DIOLATE 95.00%
1G
$ 1963.50

American Custom Chemicals Corporation
2-METHYLQUINOXALINEDIIUM-1,4-DIOLATE 95.00%
100MG
$ 750.75

Total 9 raw suppliers

Chemical Property of 2-Methylquinoxaline 1,4-dioxide

Chemical Property:

PSA：50.92000
LogP:2.00520
Storage Temp.:Refrigerator, under inert atmosphere
Solubility.:Chloroform (Slightly), Methanol (Slightly)
XLogP3:0.3
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:0
Exact Mass:176.058577502
Heavy Atom Count:13
Complexity:262

Purity/Quality:

99% ^*data from raw suppliers

2-METHYLQUINOXALINE 1,4-DIOXIDE ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC1=C[N+](=O)C2=CC=CC=C2N1[O-]
Uses Quinoxaline derivative. Bactericidal activity.

Technology Process of 2-Methylquinoxaline 1,4-dioxide

There total 18 articles about 2-Methylquinoxaline 1,4-dioxide 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: 90.0%

: 7251-61-8
2-methylquinoxaline

: 6639-86-7
2-methylquinoxaline 1,4-dioxide

Guidance literature:: With HOF* CH₃CN; In chloroform; at 0 ℃; for 0.0333333h;
DOI:10.1021/jo0608016

Reference yield: 90.0%

: 18916-45-5
3-Methylquinoxaline 1-Oxide

: 6639-86-7
2-methylquinoxaline 1,4-dioxide

Guidance literature:: With 3-chloro-benzenecarboperoxoic acid; In dichloromethane; for 16h; Ambient temperature;
DOI:10.1021/jo01298a030

Reference yield: 75.0%

: 480-96-6,68100-26-5
benzofurazan oxide

: 123-38-6
propionaldehyde

: 6639-86-7
2-methylquinoxaline 1,4-dioxide

Guidance literature:: benzofurazan oxide; With β‐cyclodextrin; In methanol; water; for 0.5h;

propionaldehyde; In methanol; water; at 20 ℃; for 0.416667h;
DOI:10.1080/00397911.2010.517371