N,3-Diphenyl[1,2,4]triazolo[3,4-b][1,3,4]thiadiazol-6-amine

Base Information

Chemical Name:N,3-Diphenyl[1,2,4]triazolo[3,4-b][1,3,4]thiadiazol-6-amine
CAS No.:113486-75-2
Molecular Formula:C₁₅H₁₁N₅S
Molecular Weight:293.352
Hs Code.:
DSSTox Substance ID:DTXSID90554446
Wikidata:Q82435442
Mol file:113486-75-2.mol

Synonyms:113486-75-2;DTXSID90554446;N,3-Diphenyl[1,2,4]triazolo[3,4-b][1,3,4]thiadiazol-6-amine;AKOS002822287

Suppliers and Price of N,3-Diphenyl[1,2,4]triazolo[3,4-b][1,3,4]thiadiazol-6-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 1 raw suppliers

Chemical Property of N,3-Diphenyl[1,2,4]triazolo[3,4-b][1,3,4]thiadiazol-6-amine

Chemical Property:

XLogP3:3.8
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:5
Rotatable Bond Count:3
Exact Mass:293.07351655
Heavy Atom Count:21
Complexity:343

Purity/Quality:: 99.90% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC=C(C=C1)C2=NN=C3N2N=C(S3)NC4=CC=CC=C4

Technology Process of N,3-Diphenyl[1,2,4]triazolo[3,4-b][1,3,4]thiadiazol-6-amine

There total 8 articles about N,3-Diphenyl[1,2,4]triazolo[3,4-b][1,3,4]thiadiazol-6-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: 63.0%

: 103-72-0
phenyl isothiocyanate

: 22706-11-2
3-phenyl-4-amino-5-mercapto-1,2,4-triazole

: 113486-75-2
6-phenylamino-3-phenyl-1,2,4-triazolo<3,4-b><1,3,4>thiadiazole

Guidance literature:: In N,N-dimethyl-formamide; for 24h; Heating;

Reference yield: 51.0%

: 22706-11-2
4-amino-3-phenyl-1H-1,2,4-triazole-5(4H)-thione

: 103-72-0
phenyl isothiocyanate

: 113486-75-2
6-phenylamino-3-phenyl-1,2,4-triazolo<3,4-b><1,3,4>thiadiazole

Guidance literature:: With dicyclohexyl-carbodiimide; In ethanol; for 6h; Heating;

Reference yield:

: 613-94-5
benzoic acid hydrazide

: 113486-75-2
6-phenylamino-3-phenyl-1,2,4-triazolo<3,4-b><1,3,4>thiadiazole

Guidance literature:: Multi-step reaction with 4 steps

1: NH₄OH

2: 2.) H⁺

3: NH₂-NH₂

4: 63 percent / dimethylformamide / 24 h / Heating

With ammonium hydroxide; hydrogen cation; hydrazine; In N,N-dimethyl-formamide;