Tioxazafen

Base Information

Chemical Name:Tioxazafen
CAS No.:330459-31-9
Molecular Formula:C₁₂H₈N₂OS
Molecular Weight:228.274
Hs Code.:
European Community (EC) Number:810-533-8
UNII:45442MUI4L
DSSTox Substance ID:DTXSID10186703
Nikkaji Number:J3.585.517C
Wikipedia:Tioxazafen
Wikidata:Q27225247

Synonyms:Tioxazafen;330459-31-9;3-phenyl-5-(thiophen-2-yl)-1,2,4-oxadiazole;Tioxazafen [ISO];3-phenyl-5-thiophen-2-yl-1,2,4-oxadiazole;3-Phenyl-5-(2-thienyl)-1,2,4-oxadiazole;UNII-45442MUI4L;1,2,4-Oxadiazole, 3-phenyl-5-(2-thienyl)-;45442MUI4L;EC 810-533-8;3-Phenyl-5-thiophen-2-yl-[1,2,4]oxadiazole;Cambridge id 5652963;SCHEMBL2459287;DTXSID10186703;CHEBI:131756;HMS1583K21;STK323466;AKOS000593363;MON-102100;SS-4600;HY-136240;CS-0120932;J3.585.517C;AB00091877-01;A905567;Q27225247;Z57260419

Suppliers and Price of Tioxazafen

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

Atlantic Research Chemicals
3-Phenyl-5-(thiophen-2-yl)-1,2,4-oxadiazole 95%
1gm:
$ 844.76

Total 23 raw suppliers

Chemical Property of Tioxazafen

Chemical Property:

Boiling Point:390.8±34.0 °C(Predicted)
Density:1.277±0.06 g/cm3(Predicted)
XLogP3:3.2
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:2
Exact Mass:228.03573406
Heavy Atom Count:16
Complexity:233

Purity/Quality:

99.9% ^*data from raw suppliers

3-Phenyl-5-(thiophen-2-yl)-1,2,4-oxadiazole 95% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC=C(C=C1)C2=NOC(=N2)C3=CC=CS3

Technology Process of Tioxazafen

There total 14 articles about Tioxazafen 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: 95.0%

: 5271-67-0
2-Thiophenecarbonyl chloride

: 613-92-3
N-hydroxybenzenecarboximidamide

: 330459-31-9
3-phenyl-5-(thiophen-2-yl)-1 ,2,4-oxadiazole

Guidance literature:: With tetra(n-butyl)ammonium hydroxide; sodium hydroxide; In 2-methyltetrahydrofuran; water; at 70 ℃; for 1.33333h; Solvent; Temperature; Time; Reagent/catalyst;

Reference yield: 89.0%

: 1261288-18-9
2-(dibromomethyl)thiophene

: 613-92-3
N-hydroxyl-benzamidine

: 330459-31-9
3-phenyl-5-(thiophen-2-yl)-1 ,2,4-oxadiazole

Guidance literature:: With pyridine; potassium tert-butylate; iodine; at 80 ℃; for 9h;
DOI:10.1139/cjc-2018-0333

Reference yield: 80.7%

: (Z)-N'-hydroxy-N-(thiophen-2-ylmethyl)benzimidamide

: 330459-31-9
3-phenyl-5-(thiophen-2-yl)-1 ,2,4-oxadiazole

Guidance literature:: With potassium phosphate; tetrabutylammonium perchlorate; In methanol; at 30 ℃; for 2h; Electrochemical reaction; Green chemistry;
DOI:10.1039/d1ob02040d