2-(4-aminophenyl)-5-(4-nitrophenyl)[1,2,4]triazolo[3,4-b][1,3,4]thiadiazole

Base Information

Chemical Name:2-(4-aminophenyl)-5-(4-nitrophenyl)[1,2,4]triazolo[3,4-b][1,3,4]thiadiazole
CAS No.:1185732-15-3
Molecular Formula:C₁₅H₁₀N₆O₂S
Molecular Weight:338.349
Hs Code.:

Synonyms:2-(4-aminophenyl)-5-(4-nitrophenyl)[1,2,4]triazolo[3,4-b][1,3,4]thiadiazole

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

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Chemical Property of 2-(4-aminophenyl)-5-(4-nitrophenyl)[1,2,4]triazolo[3,4-b][1,3,4]thiadiazole

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Technology Process of 2-(4-aminophenyl)-5-(4-nitrophenyl)[1,2,4]triazolo[3,4-b][1,3,4]thiadiazole

There total 1 articles about 2-(4-aminophenyl)-5-(4-nitrophenyl)[1,2,4]triazolo[3,4-b][1,3,4]thiadiazole 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%

: 36209-50-4
4-amino-5-(4-nitrophenyl)-1,2,4-triazole-3-thiol

: 150-13-0,159246-81-8,8014-65-1
4-amino-benzoic acid

: 1185732-15-3
2-(4-aminophenyl)-5-(4-nitrophenyl)[1,2,4]triazolo[3,4-b][1,3,4]thiadiazole

Guidance literature:: With PPA; at 100 - 200 ℃;
DOI:10.1002/ejoc.200900218

Reference yield: 55.0%

: 1185732-15-3
2-(4-aminophenyl)-5-(4-nitrophenyl)[1,2,4]triazolo[3,4-b][1,3,4]thiadiazole

: 120-07-0
2,2'-(phenylimino)bis[ethanol]

: 1422258-27-2
2-(4-{4-[N,N-bis(2-hydroxyethyl)amino]phenylazo}phenyl)-5-(4-nitrophenyl)[1,2,4]triazolo[3,4-b][1,3,4]thiadiazole

Guidance literature:: 2-(4-aminophenyl)-5-(4-nitrophenyl)[1,2,4]triazolo[3,4-b][1,3,4]thiadiazole; With hydrogenchloride; sodium nitrite; In water; at 0 - 4 ℃;

2,2'-(phenylimino)bis[ethanol]; With sodium acetate; In water; at 20 ℃; for 1h;
DOI:10.1002/ejoc.200900218