(S)-2-{[(tert-butoxy)carbonyl]amino}-4-phenoxybutyric acid methyl ester

Base Information

Chemical Name:(S)-2-{[(tert-butoxy)carbonyl]amino}-4-phenoxybutyric acid methyl ester
CAS No.:1205637-24-6
Molecular Formula:C₁₆H₂₃NO₅
Molecular Weight:309.362
Hs Code.:

Synonyms:(S)-2-{[(tert-butoxy)carbonyl]amino}-4-phenoxybutyric acid methyl ester

Suppliers and Price of (S)-2-{[(tert-butoxy)carbonyl]amino}-4-phenoxybutyric acid methyl 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
Packaging
price

Total 0 raw suppliers

Chemical Property of (S)-2-{[(tert-butoxy)carbonyl]amino}-4-phenoxybutyric acid methyl ester

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of (S)-2-{[(tert-butoxy)carbonyl]amino}-4-phenoxybutyric acid methyl ester

There total 1 articles about (S)-2-{[(tert-butoxy)carbonyl]amino}-4-phenoxybutyric acid methyl 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: 61.0%

: 120042-11-7,258351-86-9
methyl (S)-4-hydroxy-2-((tert-butoxy)carbonylamino)-butyrate

: 108-95-2,27073-41-2
phenol

: 1205637-24-6
(S)-2-{[(tert-butoxy)carbonyl]amino}-4-phenoxybutyric acid methyl ester

Guidance literature:: With di-isopropyl azodicarboxylate; triphenylphosphine; In tetrahydrofuran; at 20 ℃;

Reference yield:

: 1205637-24-6
(S)-2-{[(tert-butoxy)carbonyl]amino}-4-phenoxybutyric acid methyl ester

: 1205637-29-1
(S)-2-amino-4-phenoxybutyric acid methyl ester

Guidance literature:: (S)-2-{[(tert-butoxy)carbonyl]amino}-4-phenoxybutyric acid methyl ester; With trifluoroacetic acid; In dichloromethane; for 16h; Inert atmosphere;

With sodium hydrogencarbonate; In water;

Reference yield:

: 1205637-24-6
(S)-2-{[(tert-butoxy)carbonyl]amino}-4-phenoxybutyric acid methyl ester

: 1205637-22-4
(S)-4-(2-phenoxyethyl)-4,5-dihydrooxazol-2-ylamine

Guidance literature:: Multi-step reaction with 3 steps

1: trifluoroacetic acid / dichloromethane / 16 h / Inert atmosphere

2: lithium aluminium tetrahydride / tetrahydrofuran / 2 h / 50 °C

3: potassium carbonate / tetrahydrofuran / 18 h / Inert atmosphere

With lithium aluminium tetrahydride; potassium carbonate; trifluoroacetic acid; In tetrahydrofuran; dichloromethane;
DOI:10.1021/acsmedchemlett.5b00449