methyl (1R,2R)-2-(phenylcarbamoyl)cyclohexanecarboxylate

Base Information

Chemical Name:methyl (1R,2R)-2-(phenylcarbamoyl)cyclohexanecarboxylate
CAS No.:6938-50-7
Molecular Formula:C₁₅H₁₉NO₃
Molecular Weight:261.321
Hs Code.:

Synonyms:Cyclohexanecarboxylicacid, 2-phenylcarbamoyl-, trans-, methyl ester (5CI); NSC 404767; NSC 53970

Suppliers and Price of methyl (1R,2R)-2-(phenylcarbamoyl)cyclohexanecarboxylate

Supply Marketing:

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

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 3 raw suppliers

Chemical Property of methyl (1R,2R)-2-(phenylcarbamoyl)cyclohexanecarboxylate

Chemical Property:

Vapor Pressure:7.24E-08mmHg at 25°C
Boiling Point:437.8°C at 760 mmHg
Flash Point:218.6°C
Density:1.173g/cm³

Purity/Quality:: 99% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Technology Process of methyl (1R,2R)-2-(phenylcarbamoyl)cyclohexanecarboxylate

There total 10 articles about methyl (1R,2R)-2-(phenylcarbamoyl)cyclohexanecarboxylate 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:

: 62-53-3
aniline

: 6938-50-7
(+/-)-trans-2-phenylcarbamoyl-cyclohexanecarboxylic acid methyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: benzene

2: aqueous sodium carbonate

With sodium carbonate; benzene;

Reference yield:

: 17716-13-1,78431-28-4,92671-00-6,127932-93-8
(+/-)-cis-1-phenylcarbamoyl-cyclohexane-carboxylic acid-⁽²⁾

: 6938-50-7
(+/-)-trans-2-phenylcarbamoyl-cyclohexanecarboxylic acid methyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: ethanolic KOH-solution

2: aqueous sodium carbonate

With potassium hydroxide; sodium carbonate;