98541-64-1
(S)-3-(Tert-Butoxycarbonylamino)-2-Oxetanone
CAS: 98541-64-1
Molecular Formula: C8H13NO4
98541-64-1 - Names and Identifiers
98541-64-1 - Physico-chemical Properties
| Molecular Formula | C8H13NO4 |
| Molar Mass | 187.19 |
| Density | 1.18±0.1 g/cm3(Predicted) |
| Melting Point | 117-119 °C |
| Boling Point | 319.0±31.0 °C(Predicted) |
| Solubility | Acetonitrile (Slightly), Chloroform (Slightly), DMSO (Slightly), Methanol (Slig |
| Appearance | Solid |
| Color | White to Off-White |
| pKa | 10.53±0.20(Predicted) |
| Storage Condition | Inert atmosphere,Store in freezer, under -20°C |
| Stability | Unstable in Solution |
| Refractive Index | -26 ° (C=1, CH3CN) |
| MDL | MFCD01318414 |
98541-64-1 - Risk and Safety
| Safety Description | 24/25 - Avoid contact with skin and eyes. |
| HS Code | 29322090 |
98541-64-1 - Reference Information
| Introduction | N-(tert-butoxycarbonyl)-L-serine-beta-lactone is L-Serine-beta-lactone The amino-protected compound of lactone is often used in the synthesis of pharmaceutical and chemical intermediates and is an important ß-lactone inhibitor. |
| preparation | N-(tert-butoxycarbonyl)-L-serine-β-lactone is made of L-aminoalanine as the starting material and is protected by tert-butoxycarbonyl for amino groups, the target compound N-(tert-butoxycarbonyl)-L-serine-β-lactone is prepared by intramolecular cyclization catalysis of citric acid. The synthesis reaction formula is as follows: |
| use | an important beta-lactone inhibitor. |
Last Update：2024-04-10 22:40:09
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