(S)-tert-Butyl (4-oxobutan-2-yl)carbamate
97%
- Product Code: 123689
CAS:
118173-26-5
| Molecular Weight: | 187.24 g./mol | Molecular Formula: | C₉H₁₇NO₃ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD30162643 | |
| Melting Point: | Boiling Point: | 279.9±23.0 °C(Predicted) | |
| Density: | 1.000±0.06 g/cm3(Predicted) | Storage Condition: | -20°C, inert gas |
Product Description:
(S)-tert-Butyl (4-oxobutan-2-yl)carbamate is primarily utilized in organic synthesis as a key intermediate in the production of various pharmaceuticals and bioactive compounds. Its structure, featuring both a tert-butyl carbamate group and a ketone functionality, makes it a versatile building block for constructing complex molecules. It is often employed in the synthesis of chiral compounds, particularly in the development of drugs targeting neurological disorders, cancer, and infectious diseases. The tert-butyl group provides steric protection during synthetic processes, while the ketone moiety allows for further functionalization through reactions like reduction, nucleophilic addition, or condensation. Additionally, its chiral center enables the creation of enantiomerically pure substances, which are crucial for ensuring the efficacy and safety of many therapeutic agents.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿3,087.00 |
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| 0.250 | 10-20 days | ฿5,247.00 |
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| 1.000 | 10-20 days | ฿14,157.00 |
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(S)-tert-Butyl (4-oxobutan-2-yl)carbamate
(S)-tert-Butyl (4-oxobutan-2-yl)carbamate is primarily utilized in organic synthesis as a key intermediate in the production of various pharmaceuticals and bioactive compounds. Its structure, featuring both a tert-butyl carbamate group and a ketone functionality, makes it a versatile building block for constructing complex molecules. It is often employed in the synthesis of chiral compounds, particularly in the development of drugs targeting neurological disorders, cancer, and infectious diseases. The tert-butyl group provides steric protection during synthetic processes, while the ketone moiety allows for further functionalization through reactions like reduction, nucleophilic addition, or condensation. Additionally, its chiral center enables the creation of enantiomerically pure substances, which are crucial for ensuring the efficacy and safety of many therapeutic agents.
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