-N-(4-methoxyphenyl)phenylketenimin

Base Information

Chemical Name:-N-(4-methoxyphenyl)phenylketenimin
CAS No.:77596-50-0
Molecular Formula:C₁₉H₁₇N₃O
Molecular Weight:303.363
Hs Code.:

<N-(Cyanmethyl)acetimidoyl>-N-(4-methoxyphenyl)phenylketenimin

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Suppliers and Price of -N-(4-methoxyphenyl)phenylketenimin

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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-methoxyphenyl)phenylketenimin

Chemical Property:

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Technology Process of -N-(4-methoxyphenyl)phenylketenimin

There total 3 articles about -N-(4-methoxyphenyl)phenylketenimin 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: 64.0%

: 77596-35-1
5-(4-Methoxyphenylimino)-3-methyl-4-phenyl-3-isothiazolin-2-acetonitril

: 77596-50-0
-N-(4-methoxyphenyl)phenylketenimin

Guidance literature:: With tributylphosphine; In dichloromethane; di-isopropyl ether; Ambient temperature;

Reference yield:

: 75184-18-8
N-(4-Methoxyphenyl)-3-oxo-2-(phenyl)thiobuttersaeure-amid

: 77596-50-0
-N-(4-methoxyphenyl)phenylketenimin

Guidance literature:: Multi-step reaction with 3 steps

1: 1) N(C₂H₅)3, 2) H₂O / 1) ethanol, 24 h, 2) ethanol, 0 deg C

2: 80 percent / Br₂, pyridine / ethyl acetate / 0 - 10 °C

3: 64 percent / tributylphosphane / diisopropyl ether; CH₂Cl₂ / Ambient temperature

With pyridine; tributylphosphine; water; bromine; triethylamine; In dichloromethane; di-isopropyl ether; ethyl acetate;

Reference yield:

: 77596-17-9
3-<(Cyanmethyl)amino>-N-(4-methoxyphenyl)-2-phenylcrotonthioamid

: 77596-50-0
-N-(4-methoxyphenyl)phenylketenimin

Guidance literature:: Multi-step reaction with 2 steps

1: 80 percent / Br₂, pyridine / ethyl acetate / 0 - 10 °C

2: 64 percent / tributylphosphane / diisopropyl ether; CH₂Cl₂ / Ambient temperature

With pyridine; tributylphosphine; bromine; In dichloromethane; di-isopropyl ether; ethyl acetate;