Phenol, 2-[5-(phenylamino)-1,3,4-thiadiazol-2-yl]-

Base Information

Chemical Name:Phenol, 2-[5-(phenylamino)-1,3,4-thiadiazol-2-yl]-
CAS No.:94565-97-6
Molecular Formula:C14H11N3OS
Molecular Weight:269.327
Hs Code.:

Synonyms:2-(anilino-[1,3,4]thiadiazol-2-yl)-phenol;2-(5-anilino-1,3,4-thiadiazole-2-yl)phenol;Phenol,2-[5-(phenylamino)-1,3,4-thiadiazol-2-yl];

Suppliers and Price of Phenol, 2-[5-(phenylamino)-1,3,4-thiadiazol-2-yl]-

Supply Marketing:

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

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Chemical Property of Phenol, 2-[5-(phenylamino)-1,3,4-thiadiazol-2-yl]-

Chemical Property:

Melting Point:203 °C
Boiling Point:461.1±47.0 °C(Predicted)
PSA：89.25000
Density:1.380±0.06 g/cm3(Predicted)
LogP:1.76360

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Technology Process of Phenol, 2-[5-(phenylamino)-1,3,4-thiadiazol-2-yl]-

There total 9 articles about Phenol, 2-[5-(phenylamino)-1,3,4-thiadiazol-2-yl]- 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%

: 37536-32-6
2-(2-hydroxybenzoyl)-N-phenylhydrazincarbothioamide

: 94565-97-6
5-(2-hydroxyphenyl)-2-phenylamino-2,4-dihydro-3H-1,3,4-thiadiazole

Guidance literature:: In ethanol; sulfuric acid; 1.) 15 min; 2.) reflux, 30 min;

Reference yield: 84.0%

: 90-02-8
salicylaldehyde

: 103-72-0
phenyl isothiocyanate

: 94565-97-6
5-(2-hydroxyphenyl)-2-phenylamino-2,4-dihydro-3H-1,3,4-thiadiazole

Guidance literature:: With iron(III) chloride; hydrazine hydrate; In water; for 0.0666667h; Microwave irradiation; Sonication; Green chemistry;
DOI:10.1007/s00706-012-0846-x