(4-Methoxy-phenyl)-(2-oxo-2-phenyl-ethyl)-thiocarbamic acid O-phenyl ester

Base Information

Chemical Name:(4-Methoxy-phenyl)-(2-oxo-2-phenyl-ethyl)-thiocarbamic acid O-phenyl ester
CAS No.:154551-58-3
Molecular Formula:C₂₂H₁₉NO₃S
Molecular Weight:377.464
Hs Code.:

Synonyms:(4-Methoxy-phenyl)-(2-oxo-2-phenyl-ethyl)-thiocarbamic acid O-phenyl ester

Suppliers and Price of (4-Methoxy-phenyl)-(2-oxo-2-phenyl-ethyl)-thiocarbamic acid O-phenyl ester

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

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Chemicals and raw materials
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price

Total 2 raw suppliers

Chemical Property of (4-Methoxy-phenyl)-(2-oxo-2-phenyl-ethyl)-thiocarbamic acid O-phenyl ester

Chemical Property:

Purity/Quality:: 98% ^*data from raw suppliers

Safty Information:

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Hazard Codes:

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Useful:

Technology Process of (4-Methoxy-phenyl)-(2-oxo-2-phenyl-ethyl)-thiocarbamic acid O-phenyl ester

There total 3 articles about (4-Methoxy-phenyl)-(2-oxo-2-phenyl-ethyl)-thiocarbamic acid O-phenyl ester 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: 92.0%

: 5883-82-9
2-((4-methoxyphenyl)amino)-1-phenylethanone

: 1005-56-7
phenylcarbonochloridothioate

: 154551-58-3
(4-Methoxy-phenyl)-(2-oxo-2-phenyl-ethyl)-thiocarbamic acid O-phenyl ester

Guidance literature:: With potassium carbonate; In dichloromethane; for 12h; Ambient temperature;

Reference yield:

: 104-94-9
4-methoxy-aniline

: 154551-58-3
(4-Methoxy-phenyl)-(2-oxo-2-phenyl-ethyl)-thiocarbamic acid O-phenyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: 85 percent / diethyl ether / Ambient temperature

2: 92 percent / K₂CO₃ / CH₂Cl₂ / 12 h / Ambient temperature

With potassium carbonate; In diethyl ether; dichloromethane;

Reference yield:

: 70-11-1
α-bromoacetophenone

: 154551-58-3
(4-Methoxy-phenyl)-(2-oxo-2-phenyl-ethyl)-thiocarbamic acid O-phenyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: 85 percent / diethyl ether / Ambient temperature

2: 92 percent / K₂CO₃ / CH₂Cl₂ / 12 h / Ambient temperature

With potassium carbonate; In diethyl ether; dichloromethane;