tert-Butyl N-[(1S)-2-(methanesulfonyloxy)-1-phenylethyl]carbamate
95%
- Product Code: 82863
CAS:
110143-62-9
| Molecular Weight: | 315.39 g./mol | Molecular Formula: | C₁₄H₂₁NO₅S |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD22420311 | |
| Melting Point: | 113-115 °C | Boiling Point: | 497.2±45.0 °C(Predicted) |
| Density: | 1.204±0.06 g/cm3(Predicted) | Storage Condition: | room temperature |
Product Description:
This compound is primarily utilized in organic synthesis as an intermediate for the preparation of more complex molecules, particularly in pharmaceutical research. It plays a key role in the synthesis of chiral compounds, often serving as a protected form of an amine group during multi-step reactions. The methanesulfonyloxy group in the structure makes it a useful precursor for nucleophilic substitution reactions, enabling the introduction of various functional groups. Its application is significant in the development of enantiomerically pure drugs, where the chiral center is crucial for biological activity. Additionally, it is employed in peptide chemistry for the protection of amino acids, ensuring selective reactivity in peptide bond formation.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿6,300.00 |
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| 0.250 | 10-20 days | ฿10,800.00 |
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| 1.000 | 10-20 days | ฿21,294.00 |
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tert-Butyl N-[(1S)-2-(methanesulfonyloxy)-1-phenylethyl]carbamate
This compound is primarily utilized in organic synthesis as an intermediate for the preparation of more complex molecules, particularly in pharmaceutical research. It plays a key role in the synthesis of chiral compounds, often serving as a protected form of an amine group during multi-step reactions. The methanesulfonyloxy group in the structure makes it a useful precursor for nucleophilic substitution reactions, enabling the introduction of various functional groups. Its application is significant in the development of enantiomerically pure drugs, where the chiral center is crucial for biological activity. Additionally, it is employed in peptide chemistry for the protection of amino acids, ensuring selective reactivity in peptide bond formation.
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