N-(4-(4-chlorophenyl)-3-phenyl-1,3-thiazol-2(3H)-ylidene)-N-phenylamine

Base Information

Chemical Name:N-(4-(4-chlorophenyl)-3-phenyl-1,3-thiazol-2(3H)-ylidene)-N-phenylamine
CAS No.:1354258-82-4
Molecular Formula:C₂₁H₁₅ClN₂S
Molecular Weight:362.882
Hs Code.:
Mol file:1354258-82-4.mol

Synonyms:N-[4-(4-chlorophenyl)-3-phenylthiazol-2(3H)-ylidene]-phenylamine

Suppliers and Price of N-(4-(4-chlorophenyl)-3-phenyl-1,3-thiazol-2(3H)-ylidene)-N-phenylamine

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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 N-(4-(4-chlorophenyl)-3-phenyl-1,3-thiazol-2(3H)-ylidene)-N-phenylamine

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Technology Process of N-(4-(4-chlorophenyl)-3-phenyl-1,3-thiazol-2(3H)-ylidene)-N-phenylamine

There total 3 articles about N-(4-(4-chlorophenyl)-3-phenyl-1,3-thiazol-2(3H)-ylidene)-N-phenylamine 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: 70.0%

: 103-72-0
phenyl isothiocyanate

: 62-53-3
aniline

: 536-38-9
4-chlorobenzoylmethyl bromide

: 1354258-82-4
N-[4-(4-chlorophenyl)-3-phenylthiazol-2(3H)-ylidene]-phenylamine

Guidance literature:: With triethylamine; In ethanol; for 0.166667h; regioselective reaction; Reflux;
DOI:10.1016/j.tetlet.2011.11.017

Reference yield:

: 89891-82-7
(4-chlorophenyl)ethynyl iodide

: 103-72-0
phenyl isothiocyanate

: 62-53-3
aniline

: 1354258-82-4
N-[4-(4-chlorophenyl)-3-phenylthiazol-2(3H)-ylidene]-phenylamine

Guidance literature:: With acetic acid; In water; at 70 ℃; for 1h; regioselective reaction;
DOI:10.1055/s-0035-1560502

Reference yield:

: 873-73-4
4-n-chlorophenylacetylene

: 1354258-82-4
N-[4-(4-chlorophenyl)-3-phenylthiazol-2(3H)-ylidene]-phenylamine

Guidance literature:: Multi-step reaction with 2 steps

1: ammonium iodide; dihydrogen peroxide; acetic acid / water / 20 °C

2: acetic acid / water / 1 h / 70 °C

With ammonium iodide; dihydrogen peroxide; acetic acid; In water;
DOI:10.1055/s-0035-1560502