5-(2,4-Dichlorophenyl)-1,3,4-oxadiazol-2-amine

Base Information

Chemical Name:5-(2,4-Dichlorophenyl)-1,3,4-oxadiazol-2-amine
CAS No.:60160-13-6
Molecular Formula:C8H5Cl2N3O
Molecular Weight:230.053
Hs Code.:
DSSTox Substance ID:DTXSID00406487
Nikkaji Number:J3.406.822D
Wikidata:Q82211467

Synonyms:5-(2,4-dichlorophenyl)-1,3,4-oxadiazol-2-amine;60160-13-6;1,3,4-Oxadiazol-2-amine, 5-(2,4-dichlorophenyl)-;F2146-0617;DTXSID00406487;MFCD00099617;AKOS000159982;EN300-118527;Z285233824

Suppliers and Price of 5-(2,4-Dichlorophenyl)-1,3,4-oxadiazol-2-amine

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 5 raw suppliers

Chemical Property of 5-(2,4-Dichlorophenyl)-1,3,4-oxadiazol-2-amine

Chemical Property:

XLogP3:2.3
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:1
Exact Mass:228.9809672
Heavy Atom Count:14
Complexity:207

Purity/Quality:: NLT 98% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC(=C(C=C1Cl)Cl)C2=NN=C(O2)N

Technology Process of 5-(2,4-Dichlorophenyl)-1,3,4-oxadiazol-2-amine

There total 3 articles about 5-(2,4-Dichlorophenyl)-1,3,4-oxadiazol-2-amine 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: 82.0%

: 62036-34-4
C₈H₇Cl₂N₃O

: 60160-13-6
2-amino-5-(2,4-dichlorophenyl)-1,3,4-oxadiazole

Guidance literature:: With lithium perchlorate; acetic acid; at 25 ℃; for 5h; Electrolysis;
DOI:10.4067/S0717-97072010000100030

Reference yield: 70.0%

: 26036-09-9
1-(2,4-dichlorobenzoyl)-3-thiosemicarbazide

: 60160-13-6
2-amino-5-(2,4-dichlorophenyl)-1,3,4-oxadiazole

Guidance literature:: With sodium hydroxide; iodine; potassium iodide; In water; Heating;

Reference yield:

: 874-42-0
2,4-dichlorobenzaldeyhde

: 60160-13-6
2-amino-5-(2,4-dichlorophenyl)-1,3,4-oxadiazole

Guidance literature:: Multi-step reaction with 2 steps

1: sodium acetate / water; methanol / 0.17 h / 20 °C

2: potassium carbonate; iodine / 1,4-dioxane / 80 °C

With iodine; sodium acetate; potassium carbonate; In 1,4-dioxane; methanol; water;
DOI:10.1021/jo502518c