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| | (S)-3-Boc-Amino-gamma-butyrolactone Basic information |
| Product Name: | (S)-3-Boc-Amino-gamma-butyrolactone | | Synonyms: | (S)-3-Boc-AMino-g-butyrolactone;(S)-3-BOC-AMINOTETRAHYDROFURAN-5-ONE;(S)-3-BOC-AMINO-GAMMA-BUTYROLACTONE;(S)-3- BOC-AMINO -γ-BUTYROLACTONE;(S)-tert-Butyl (5-oxotetrahydrofuran-3-yl)carbaMate;CarbaMic acid, [(3S)-tetrahydro-5-oxo-3-furanyl]-, 1,1-diMethylethyl ester;(S)-3-Boc-AMino-GaMMa-ButyrolaCLone;tert-Butyl [(3S)-5-oxotetrahydrofuran-3-yl]carbamate | | CAS: | 104227-71-6 | | MF: | C9H15NO4 | | MW: | 201.22 | | EINECS: | | | Product Categories: | pharmacetical;Tetrahydrofuran Series | | Mol File: | 104227-71-6.mol |  |
| | (S)-3-Boc-Amino-gamma-butyrolactone Chemical Properties |
| Melting point | 113-114 °C | | Boiling point | 363.7±31.0 °C(Predicted) | | density | 1.15±0.1 g/cm3(Predicted) | | storage temp. | 2-8°C | | pka | 11.08±0.20(Predicted) |
| Safety Statements | 24/25 | | HS Code | 29321900 |
| | (S)-3-Boc-Amino-gamma-butyrolactone Usage And Synthesis |
| Uses | (S)-tert-Butyl (5-Oxotetrahydrofuran-3-yl)carbamate is a useful reagent in the study of asymmetric synthesis of protected amino acids consitutnes of cyclomarin A. |
| | (S)-3-Boc-Amino-gamma-butyrolactone Preparation Products And Raw materials |
| Raw materials | 5,7-Dioxa-2-aza-10-silaundecanoic acid, 3-(chloromethyl)-10,10-dimethyl-, 1,1-dimethylethyl ester, (3R)--->5,7-Dioxa-2-aza-10-silaundecanoic acid, 3-(2-methoxy-2-oxoethyl)-10,10-dimethyl-, 1,1-dimethylethyl ester, (3S)--->(R)-3-BOC-AMINO-GAMMA-BUTYROLACTONE-->(S)-N-BOC-3-AMINO-4-HYDROXYBUTYRIC ACID-->Carbamic acid, [(1R)-2-chloro-1-(hydroxymethyl)ethyl]-, 1,1-dimethylethyl ester-->METHYL N-BOC-3-CHLORO-L-ALANINATE
-->Benzyl (S)-(-)-tetrahydro-5-oxo-3-furanylcarbamate-->Butanoic acid, 3-[[(1,1-diMethylethoxy)carbonyl]aMino]-4-hydroxy-, Methyl ester, (3S)--->Boc-L-serine methyl ester-->Di-tert-butyl dicarbonate | | Preparation Products | (S)-(-)-alpha-(Boc-Amino)-gamma-butyrolactone |
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