2-({2-[4-(4-methoxyphenyl)-1,3-thiazol-2-yl]hydrazinylidene}-methyl)phenol

Base Information

Chemical Name:2-({2-[4-(4-methoxyphenyl)-1,3-thiazol-2-yl]hydrazinylidene}-methyl)phenol
CAS No.:896064-76-9
Molecular Formula:C₁₇H₁₅N₃O₂S
Molecular Weight:325.391
Hs Code.:

Synonyms:2-({2-[4-(4-methoxyphenyl)-1,3-thiazol-2-yl]hydrazinylidene}-methyl)phenol

Suppliers and Price of 2-({2-[4-(4-methoxyphenyl)-1,3-thiazol-2-yl]hydrazinylidene}-methyl)phenol

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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-({2-[4-(4-methoxyphenyl)-1,3-thiazol-2-yl]hydrazinylidene}-methyl)phenol

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Technology Process of 2-({2-[4-(4-methoxyphenyl)-1,3-thiazol-2-yl]hydrazinylidene}-methyl)phenol

There total 2 articles about 2-({2-[4-(4-methoxyphenyl)-1,3-thiazol-2-yl]hydrazinylidene}-methyl)phenol 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: 75.0%

: 5351-90-6,17149-00-7
salicylaldehyde thiosemicarbazone

: 2632-13-5
2-Bromo-4'-methoxyacetophenone

: 896064-76-9
2-({2-[4-(4-methoxyphenyl)-1,3-thiazol-2-yl]hydrazinylidene}-methyl)phenol

Guidance literature:: salicylaldehyde thiosemicarbazone; 2-Bromo-4'-methoxyacetophenone; In methanol; ethanol; Reflux;

With sodium hydrogencarbonate; potassium carbonate; In water;
DOI:10.1016/j.ejmech.2009.11.008

Reference yield:

: 90-02-8
salicylaldehyde

: 896064-76-9
2-({2-[4-(4-methoxyphenyl)-1,3-thiazol-2-yl]hydrazinylidene}-methyl)phenol

Guidance literature:: Multi-step reaction with 2 steps

1: acetic acid / ethanol; water / Reflux

2: methanol / Reflux

With acetic acid; In methanol; ethanol; water;
DOI:10.1007/s11243-010-9412-8