2-phenylethyl 4-(2-bromo-3,6-dimethoxyphenyl)-6-methyl-2-oxo-1,2,3,4-tetrahydropyrimidine-5-carboxylate

Base Information

Chemical Name:2-phenylethyl 4-(2-bromo-3,6-dimethoxyphenyl)-6-methyl-2-oxo-1,2,3,4-tetrahydropyrimidine-5-carboxylate
CAS No.:5472-74-2
Molecular Formula:C₁₄H₁₇NO₅S
Molecular Weight:311.359
Hs Code.:

Synonyms:Alanine,N-benzoyl-3-[(carboxymethyl)thio]-, dimethyl ester (6CI,7CI); NSC 29414

Suppliers and Price of 2-phenylethyl 4-(2-bromo-3,6-dimethoxyphenyl)-6-methyl-2-oxo-1,2,3,4-tetrahydropyrimidine-5-carboxylate

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 6 raw suppliers

Chemical Property of 2-phenylethyl 4-(2-bromo-3,6-dimethoxyphenyl)-6-methyl-2-oxo-1,2,3,4-tetrahydropyrimidine-5-carboxylate

Chemical Property:

Vapor Pressure:6.18E-13mmHg at 25°C
Boiling Point:568.4°C at 760 mmHg
Flash Point:297.6°C
Density:1.367g/cm³

Purity/Quality:: 85.0-99.8% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Technology Process of 2-phenylethyl 4-(2-bromo-3,6-dimethoxyphenyl)-6-methyl-2-oxo-1,2,3,4-tetrahydropyrimidine-5-carboxylate

There total 5 articles about 2-phenylethyl 4-(2-bromo-3,6-dimethoxyphenyl)-6-methyl-2-oxo-1,2,3,4-tetrahydropyrimidine-5-carboxylate 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:

: 638-23-3,2387-59-9,29433-95-2
carbocisteine

: 5472-74-2
N-benzoyl-S-methoxycarbonylmethyl-L-cysteine methyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: aq. NaOH solution

2: sulfuric acid

With sodium hydroxide; sulfuric acid;
DOI:10.1021/ja01238a042

Reference yield:

: 67-56-1
methanol

: 6332-29-2
N-benzoyl-S-carboxymethyl-L-cysteine

: 5472-74-2
N-benzoyl-S-methoxycarbonylmethyl-L-cysteine methyl ester

Guidance literature:: With sulfuric acid;
DOI:10.1021/ja01238a042

Reference yield:

: 98-88-4
benzoyl chloride

: 5472-74-2
N-benzoyl-S-methoxycarbonylmethyl-L-cysteine methyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: aq. NaOH solution

2: sulfuric acid

With sodium hydroxide; sulfuric acid;
DOI:10.1021/ja01238a042