4-Benzenesulfonyl-3-methyl-furazan 2-oxide

Base Information

Chemical Name:4-Benzenesulfonyl-3-methyl-furazan 2-oxide
CAS No.:49739-41-5
Molecular Formula:C9H8N2O4S
Molecular Weight:240.24
Hs Code.:
DSSTox Substance ID:DTXSID20416008
Nikkaji Number:J480.688C
Wikidata:Q82225122
ChEMBL ID:CHEMBL320995

Synonyms:4-methyl-3-(phenylsulfonyl)furoxan;4-methyl-3-phenyl sulfonylfuroxan;4-MPSF;S 35b;S35b

Suppliers and Price of 4-Benzenesulfonyl-3-methyl-furazan 2-oxide

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 3 raw suppliers

Chemical Property of 4-Benzenesulfonyl-3-methyl-furazan 2-oxide

Chemical Property:

XLogP3:2
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:5
Rotatable Bond Count:2
Exact Mass:240.02047791
Heavy Atom Count:16
Complexity:334

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

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC1=[N+](ON=C1S(=O)(=O)C2=CC=CC=C2)[O-]

Technology Process of 4-Benzenesulfonyl-3-methyl-furazan 2-oxide

There total 5 articles about 4-Benzenesulfonyl-3-methyl-furazan 2-oxide 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: 87.0%

: 49739-36-8
3-methyl-4-(phenylthio)furoxan

: 49739-41-5
3-methyl-4-phenylsulphonylfuroxan

Guidance literature:: With dihydrogen peroxide; In trifluoroacetic acid; for 1h;
DOI:10.1021/jm00095a028

Reference yield:

: 108-98-5
thiophenol

: 49739-41-5
3-methyl-4-phenylsulphonylfuroxan

Guidance literature:: Multi-step reaction with 3 steps

1: 92 percent / triethylamine / diethyl ether / 1 h / Ambient temperature

2: 40 percent / N₂O₄ / diethyl ether / 17 h / 0 - 20 °C

3: 87 percent / 81percent H₂O₂ / trifluoroacetic acid / 1 h

With dihydrogen peroxide; dinitrogen tetraoxide; triethylamine; In diethyl ether; trifluoroacetic acid;
DOI:10.1021/jm00095a028

Reference yield:

: 142764-04-3
N-Hydroxy-2-[(E)-hydroxyimino]-thiopropionimidic acid phenyl ester

: 49739-41-5
3-methyl-4-phenylsulphonylfuroxan

Guidance literature:: Multi-step reaction with 2 steps

1: 40 percent / N₂O₄ / diethyl ether / 17 h / 0 - 20 °C

2: 87 percent / 81percent H₂O₂ / trifluoroacetic acid / 1 h

With dihydrogen peroxide; dinitrogen tetraoxide; In diethyl ether; trifluoroacetic acid;
DOI:10.1021/jm00095a028