4-(4-fluorophenyl)-2-[-2-(1-furan-2-ylethylidene)-hydrazino]-1,3-thiazole

Base Information

Chemical Name:4-(4-fluorophenyl)-2-[-2-(1-furan-2-ylethylidene)-hydrazino]-1,3-thiazole
CAS No.:1416453-54-7
Molecular Formula:C₁₅H₁₂FN₃OS
Molecular Weight:301.344
Hs Code.:

Synonyms:4-(4-fluorophenyl)-2-[-2-(1-furan-2-ylethylidene)-hydrazino]-1,3-thiazole

Suppliers and Price of 4-(4-fluorophenyl)-2-[-2-(1-furan-2-ylethylidene)-hydrazino]-1,3-thiazole

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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 4-(4-fluorophenyl)-2-[-2-(1-furan-2-ylethylidene)-hydrazino]-1,3-thiazole

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Technology Process of 4-(4-fluorophenyl)-2-[-2-(1-furan-2-ylethylidene)-hydrazino]-1,3-thiazole

There total 2 articles about 4-(4-fluorophenyl)-2-[-2-(1-furan-2-ylethylidene)-hydrazino]-1,3-thiazole 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: 80.0%

: 1192-62-7,80145-44-4
1-(2-furyl)-1-ethanone

: 79-19-6
thiosemicarbazide

: 403-29-2
2-bromo-4'-fluoroacetophenone

: 1416453-54-7
4-(4-fluorophenyl)-2-[-2-(1-furan-2-ylethylidene)-hydrazino]-1,3-thiazole

Guidance literature:: With hydrogen bromide; for 0.333333h; Microwave irradiation; Green chemistry;
DOI:10.14233/ajchem.2016.19603

Reference yield:

: 403-42-9
1-(4-fluorophenyl)ethanone

: 1416453-54-7
4-(4-fluorophenyl)-2-[-2-(1-furan-2-ylethylidene)-hydrazino]-1,3-thiazole

Guidance literature:: Multi-step reaction with 2 steps

1: bromine; acetic acid / Microwave irradiation

2: hydrogen bromide / 0.33 h / Microwave irradiation; Green chemistry

With hydrogen bromide; bromine; acetic acid; 2: |Hantzsch Thiazole Synthesis;
DOI:10.14233/ajchem.2016.19603