3-Methyl-4-phenylsulfinyl-1,2,5-oxadiazole

Base Information

Chemical Name:3-Methyl-4-phenylsulfinyl-1,2,5-oxadiazole
CAS No.:145409-22-9
Molecular Formula:C₉H₈N₂O₂S
Molecular Weight:208.241
Hs Code.:
DSSTox Substance ID:DTXSID20875853
Nikkaji Number:J492.074K
ChEMBL ID:CHEMBL112820

Synonyms:145409-22-9;CHEMBL112820;Furazan, methyl(phenylsulfinyl)-;DTXSID20875853;3-Methyl-4-phenylsulfinyl-1,2,5-oxadiazole

Suppliers and Price of 3-Methyl-4-phenylsulfinyl-1,2,5-oxadiazole

Supply Marketing:

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

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Chemical Property of 3-Methyl-4-phenylsulfinyl-1,2,5-oxadiazole

Chemical Property:

XLogP3:1.8
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:5
Rotatable Bond Count:2
Exact Mass:208.03064868
Heavy Atom Count:14
Complexity:219

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CC1=NON=C1S(=O)C2=CC=CC=C2

Technology Process of 3-Methyl-4-phenylsulfinyl-1,2,5-oxadiazole

There total 3 articles about 3-Methyl-4-phenylsulfinyl-1,2,5-oxadiazole 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: 35.0%

: 50275-23-5
3-methyl-4-phenylsulfanyl-furazan

: 145409-22-9
3-methyl-4-(phenylsulfinyl)furazan

Guidance literature:: With dihydrogen peroxide; In acetic acid; for 48h; Ambient temperature;
DOI:10.1021/jm00095a028

Reference yield:

: 108-98-5
thiophenol

: 145409-22-9
3-methyl-4-(phenylsulfinyl)furazan

Guidance literature:: Multi-step reaction with 3 steps

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

2: 1.) N₂O₂, 2.) trimethyl phosphite / 1.) ether, 0-20 deg C, 17 h

3: 35 percent / 30percent aq. H₂O₂ / acetic acid / 48 h / Ambient temperature

With N-oxo-N-nitrosoamine; dihydrogen peroxide; triethylamine; phosphorous acid trimethyl ester; In diethyl ether; acetic acid;
DOI:10.1021/jm00095a028

Reference yield:

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

: 145409-22-9
3-methyl-4-(phenylsulfinyl)furazan

Guidance literature:: Multi-step reaction with 2 steps

1: 1.) N₂O₂, 2.) trimethyl phosphite / 1.) ether, 0-20 deg C, 17 h

2: 35 percent / 30percent aq. H₂O₂ / acetic acid / 48 h / Ambient temperature

With N-oxo-N-nitrosoamine; dihydrogen peroxide; phosphorous acid trimethyl ester; In acetic acid;
DOI:10.1021/jm00095a028