2-(5-methyl-3-(4-trifluoromethylphenyl)isoxazol-4-yl)-5-(4-bromophenylamino)-1,3,4-oxdiazole

Base Information

Chemical Name:2-(5-methyl-3-(4-trifluoromethylphenyl)isoxazol-4-yl)-5-(4-bromophenylamino)-1,3,4-oxdiazole
CAS No.:1421790-27-3
Molecular Formula:C₁₉H₁₂BrF₃N₄O₂
Molecular Weight:465.229
Hs Code.:

Synonyms:2-(5-methyl-3-(4-trifluoromethylphenyl)isoxazol-4-yl)-5-(4-bromophenylamino)-1,3,4-oxdiazole

Suppliers and Price of 2-(5-methyl-3-(4-trifluoromethylphenyl)isoxazol-4-yl)-5-(4-bromophenylamino)-1,3,4-oxdiazole

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 0 raw suppliers

Chemical Property of 2-(5-methyl-3-(4-trifluoromethylphenyl)isoxazol-4-yl)-5-(4-bromophenylamino)-1,3,4-oxdiazole

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of 2-(5-methyl-3-(4-trifluoromethylphenyl)isoxazol-4-yl)-5-(4-bromophenylamino)-1,3,4-oxdiazole

There total 4 articles about 2-(5-methyl-3-(4-trifluoromethylphenyl)isoxazol-4-yl)-5-(4-bromophenylamino)-1,3,4-oxdiazole 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: 89.0%

: 1421790-37-5
C₁₉H₁₄BrF₃N₄O₂S

: 1421790-27-3
2-(5-methyl-3-(4-trifluoromethylphenyl)isoxazol-4-yl)-5-(4-bromophenylamino)-1,3,4-oxdiazole

Guidance literature:: With mercury(II) diacetate; In ethanol; for 3h; Reflux;
DOI:10.1007/s11164-013-1062-y

Reference yield:

: 66046-34-2
4-(trifluoromethyl)benzaldehyde oxime

: 1421790-27-3
2-(5-methyl-3-(4-trifluoromethylphenyl)isoxazol-4-yl)-5-(4-bromophenylamino)-1,3,4-oxdiazole

Guidance literature:: Multi-step reaction with 5 steps

1: N-chloro-succinimide / N,N-dimethyl-formamide

2: ethanol

3: hydrazine hydrate

4: ethanol / 20 °C / Reflux

5: mercury(II) diacetate / ethanol / 3 h / Reflux

With N-chloro-succinimide; mercury(II) diacetate; hydrazine hydrate; In ethanol; N,N-dimethyl-formamide;
DOI:10.1007/s11164-013-1062-y

Reference yield:

: 159693-08-0
(3-(4-trifluoromethylphenyl)-5-methyl)isoxazole-4-carboxylic acid ethyl ester

: 1421790-27-3
2-(5-methyl-3-(4-trifluoromethylphenyl)isoxazol-4-yl)-5-(4-bromophenylamino)-1,3,4-oxdiazole

Guidance literature:: Multi-step reaction with 3 steps

1: hydrazine hydrate

2: ethanol / 20 °C / Reflux

3: mercury(II) diacetate / ethanol / 3 h / Reflux

With mercury(II) diacetate; hydrazine hydrate; In ethanol;
DOI:10.1007/s11164-013-1062-y