N-(3-allyl-4-phenyl-1,3-thiazol-2(3H)-ylidene)-N-(4-methoxyphenyl)amine

Base Information

Chemical Name:N-(3-allyl-4-phenyl-1,3-thiazol-2(3H)-ylidene)-N-(4-methoxyphenyl)amine
CAS No.:352209-20-2
Molecular Formula:C₁₉H₁₈N₂OS
Molecular Weight:322.431
Hs Code.:
Mol file:352209-20-2.mol

Synonyms:3-allyl-2-(4′-methoxyphenylimino)-4-phenyl-3H-thiazole

Suppliers and Price of N-(3-allyl-4-phenyl-1,3-thiazol-2(3H)-ylidene)-N-(4-methoxyphenyl)amine

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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-(3-allyl-4-phenyl-1,3-thiazol-2(3H)-ylidene)-N-(4-methoxyphenyl)amine

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Technology Process of N-(3-allyl-4-phenyl-1,3-thiazol-2(3H)-ylidene)-N-(4-methoxyphenyl)amine

There total 3 articles about N-(3-allyl-4-phenyl-1,3-thiazol-2(3H)-ylidene)-N-(4-methoxyphenyl)amine 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: 93.0%

: 104-94-9
4-methoxy-aniline

: 70-11-1
α-bromoacetophenone

: 57-06-7,58391-87-0
N-allyl isothiocyanate

: 352209-20-2
3-allyl-2-(4′-methoxyphenylimino)-4-phenyl-3H-thiazole

Guidance literature:: With poly(4-vinylpyridine); In ethanol; at 20 ℃; for 20h; Reagent/catalyst; Temperature; regioselective reaction;
DOI:10.3987/COM-14-13122

Reference yield: 76.0%

: 1138-72-3
N-allyl-N'-(4-methoxy-phenyl)-thiourea

: 70-11-1
α-bromoacetophenone

: 352209-20-2
3-allyl-2-(4′-methoxyphenylimino)-4-phenyl-3H-thiazole

Guidance literature:: With triethylamine; In ethanol; for 2h; Reflux;
DOI:10.1016/j.molstruc.2013.02.003

Reference yield:

: 104-94-9
4-methoxy-aniline

: 352209-20-2
3-allyl-2-(4′-methoxyphenylimino)-4-phenyl-3H-thiazole

Guidance literature:: Multi-step reaction with 2 steps

1: ethanol / 28 h / 20 - 60 °C

2: triethylamine / ethanol / 2 h / Reflux

With triethylamine; In ethanol;
DOI:10.1016/j.molstruc.2013.02.003