(2S)-<<(1,1-dimethylethoxy)carbonyl>amino>-4-butanoic acid

Base Information

Chemical Name:(2S)-<<(1,1-dimethylethoxy)carbonyl>amino>-4-butanoic acid
CAS No.:1026082-99-4
Molecular Formula:C₂₀H₂₉N₃O₈
Molecular Weight:439.466
Hs Code.:

(2S)-<<(1,1-dimethylethoxy)carbonyl>amino>-4-<N'-(ethoxycarbonyl)-N-hydroxyureido>butanoic acid

Synonyms:(2S)-<<(1,1-dimethylethoxy)carbonyl>amino>-4-butanoic acid

Suppliers and Price of (2S)-<<(1,1-dimethylethoxy)carbonyl>amino>-4-butanoic acid

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 (2S)-<<(1,1-dimethylethoxy)carbonyl>amino>-4-butanoic acid

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of (2S)-<<(1,1-dimethylethoxy)carbonyl>amino>-4-butanoic acid

There total 3 articles about (2S)-<<(1,1-dimethylethoxy)carbonyl>amino>-4-butanoic acid 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: 85.0%

: 158534-33-9
(2S)-benzyl 4--2-<<(1,1-dimethylethoxy)carbonyl>amino>butanoate

: 1026082-99-4
(2S)-<<(1,1-dimethylethoxy)carbonyl>amino>-4-butanoic acid

Guidance literature:: With hydrogen; palladium on activated charcoal; In methanol; for 3h; under 1551.4 Torr;
DOI:10.1021/jm00049a013

Reference yield:

: 124994-66-7
(S)-benzyl-4-oxo-2-<<(1,1-dimethylethoxy)carbonyl>amino>butanoate

: 1026082-99-4
(2S)-<<(1,1-dimethylethoxy)carbonyl>amino>-4-butanoic acid

Guidance literature:: Multi-step reaction with 3 steps

1: 60 percent / NaBH₃CN, HCl / methanol; dioxane / 48 h / Ambient temperature

2: 90 percent / tetrahydrofuran / 0.02 h

3: 85 percent / H₂ / 10percent Pd/C / methanol / 3 h / 1551.4 Torr

With hydrogenchloride; hydrogen; sodium cyanoborohydride; palladium on activated charcoal; In tetrahydrofuran; 1,4-dioxane; methanol;
DOI:10.1021/jm00049a013

Reference yield:

: 158534-32-8
(S)-benzyl-4-<(O-benzylhydroxy)amino>-2-<<(1,1-dimethylethoxy)carbonyl>amino>butanoate

: 1026082-99-4
(2S)-<<(1,1-dimethylethoxy)carbonyl>amino>-4-butanoic acid

Guidance literature:: Multi-step reaction with 2 steps

1: 90 percent / tetrahydrofuran / 0.02 h

2: 85 percent / H₂ / 10percent Pd/C / methanol / 3 h / 1551.4 Torr

With hydrogen; palladium on activated charcoal; In tetrahydrofuran; methanol;
DOI:10.1021/jm00049a013