N-(Diphenylmethylene)-glycine 1-methylethyl ester

Base Information

Chemical Name:N-(Diphenylmethylene)-glycine 1-methylethyl ester
CAS No.:119244-11-0
Molecular Formula:C18H19NO2
Molecular Weight:281.354
Hs Code.:
Mol file:119244-11-0.mol

Synonyms:N-(diphenylmethylene)glycine isopropyl ester;diphenylidene isopropyl glycinate;Glycine,N-(diphenylmethylene)-,1-methyl ethylester;

Suppliers and Price of N-(Diphenylmethylene)-glycine 1-methylethyl ester

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
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price

Total 1 raw suppliers

Chemical Property of N-(Diphenylmethylene)-glycine 1-methylethyl ester

Chemical Property:

Melting Point:66-68℃
PSA：38.66000
LogP:3.47560

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Technology Process of N-(Diphenylmethylene)-glycine 1-methylethyl ester

There total 3 articles about N-(Diphenylmethylene)-glycine 1-methylethyl 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: 80.0%

: 1013-88-3
Benzophenone imine

: 67-63-0,8013-70-5
isopropyl alcohol

: 56-40-6,18875-39-3,25718-94-9
glycine

: 119244-11-0
N-(diphenylmethylidene)glycine isopropyl ester

Guidance literature:: isopropyl alcohol; glycine; With thionyl chloride;

Benzophenone imine;
DOI:10.1016/S0957-4166(02)00611-0

Reference yield:

: 75-30-9
2-iodo-propane

: 81167-39-7
methyl N-(diphenylmethylene)glycinate

: 119244-11-0
N-(diphenylmethylidene)glycine isopropyl ester

Guidance literature:: With sodium hydroxide; tetra(n-butyl)ammonium hydrogensulfate; Yield given. Multistep reaction; 1) CH₂Cl₂, r.t., 0.5 h, 2) CH₂Cl₂, r.t., 5 h;
DOI:10.1055/s-1991-26625