N-carbobenzoxy-γ-aminobutyrylproline

Base Information

Chemical Name:N-carbobenzoxy-γ-aminobutyrylproline
CAS No.:185757-22-6
Molecular Formula:C₁₇H₂₂N₂O₅
Molecular Weight:334.372
Hs Code.:

Synonyms:N-carbobenzoxy-γ-aminobutyrylproline

Suppliers and Price of N-carbobenzoxy-γ-aminobutyrylproline

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 0 raw suppliers

Chemical Property of N-carbobenzoxy-γ-aminobutyrylproline

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of N-carbobenzoxy-γ-aminobutyrylproline

There total 3 articles about N-carbobenzoxy-γ-aminobutyrylproline 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%

: 185757-21-5
N-carbobenzoxy-γ-aminobutyrylproline ethyl ester

: 185757-22-6
N-carbobenzoxy-γ-aminobutyrylproline

Guidance literature:: With hydrogenchloride; sodium hydroxide; In methanol; for 2h;
DOI:10.1007/BF02219346

Reference yield:

: 5105-78-2
4-(benzyloxycarbonylamino)butyric acid

: 185757-22-6
N-carbobenzoxy-γ-aminobutyrylproline

Guidance literature:: Multi-step reaction with 2 steps

1: 88 percent / ethyl acetate; dimethylformamide / 2 h / -10 - 20 °C

2: 92 percent / NaOH; HCl / methanol / 2 h

With hydrogenchloride; sodium hydroxide; In methanol; ethyl acetate; N,N-dimethyl-formamide; 1: Addition / 2: Hydrogenation;
DOI:10.1007/BF02219346

Reference yield:

: 33305-75-8,131477-20-8
L-proline ethyl ester monohydrochloride

: 185757-22-6
N-carbobenzoxy-γ-aminobutyrylproline

Guidance literature:: Multi-step reaction with 2 steps

1: 88 percent / ethyl acetate; dimethylformamide / 2 h / -10 - 20 °C

2: 92 percent / NaOH; HCl / methanol / 2 h

With hydrogenchloride; sodium hydroxide; In methanol; ethyl acetate; N,N-dimethyl-formamide; 1: Addition / 2: Hydrogenation;
DOI:10.1007/BF02219346