(S)-tert-Butyl (3-oxocyclopentyl)carbamate
97%
- Product Code: 235633
CAS:
167298-40-0
| Molecular Weight: | 199.25 g./mol | Molecular Formula: | C₁₀H₁₇NO₃ |
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| EC Number: | MDL Number: | MFCD18089809 | |
| Melting Point: | Boiling Point: | 319.2±31.0°C at 760 mmHg | |
| Density: | Storage Condition: | Room temperature, dry seal |
Product Description:
Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of biologically active compounds where chirality plays a critical role. Its structure contains both a protected amine and a ketone functional group, making it valuable in multi-step organic syntheses. The tert-butyl carbamate group serves as a protecting group for the amine, allowing selective reactions at other sites, while the ketone can undergo transformations such as reductions, Grignard additions, or reductive aminations. Commonly employed in the preparation of cyclopentane-based scaffolds found in medicinal chemistry, especially in the discovery of enzyme inhibitors and central nervous system agents. Its chiral center allows for stereoselective synthesis, enhancing the efficacy and specificity of the final drug candidates.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
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| 100mg | 10-20 days | $69.84 |
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| 250mg | 10-20 days | $132.89 |
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| 500mg | 10-20 days | $264.58 |
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| 1g | 10-20 days | $487.26 |
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| 5g | 10-20 days | $1,599.47 |
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(S)-tert-Butyl (3-oxocyclopentyl)carbamate
Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of biologically active compounds where chirality plays a critical role. Its structure contains both a protected amine and a ketone functional group, making it valuable in multi-step organic syntheses. The tert-butyl carbamate group serves as a protecting group for the amine, allowing selective reactions at other sites, while the ketone can undergo transformations such as reductions, Grignard additions, or reductive aminations. Commonly employed in the preparation of cyclopentane-based scaffolds found in medicinal chemistry, especially in the discovery of enzyme inhibitors and central nervous system agents. Its chiral center allows for stereoselective synthesis, enhancing the efficacy and specificity of the final drug candidates.
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