(R)-tert-Butyl (1-hydroxybut-3-en-2-yl)carbamate
≥95%
- Product Code: 230491
CAS:
89985-86-4
| Molecular Weight: | 187.24 g./mol | Molecular Formula: | C₉H₁₇NO₃ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD19688626 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, stored in inert gas |
Product Description:
Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) where stereochemistry plays a critical role. Its hydroxyl and carbamate functional groups allow for selective modifications, making it valuable in multi-step organic syntheses. Commonly employed in the preparation of beta-amino alcohols and other nitrogen-containing compounds with biological activity. The presence of the allyl group enables further transformations such as cross-metathesis or epoxidation, enhancing its utility in medicinal chemistry and drug discovery.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 100mg | 10-20 days | ฿6,740.00 |
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| 250mg | 10-20 days | ฿11,920.00 |
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| 1g | 10-20 days | ฿34,850.00 |
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| 5g | 10-20 days | ฿149,590.00 |
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(R)-tert-Butyl (1-hydroxybut-3-en-2-yl)carbamate
Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) where stereochemistry plays a critical role. Its hydroxyl and carbamate functional groups allow for selective modifications, making it valuable in multi-step organic syntheses. Commonly employed in the preparation of beta-amino alcohols and other nitrogen-containing compounds with biological activity. The presence of the allyl group enables further transformations such as cross-metathesis or epoxidation, enhancing its utility in medicinal chemistry and drug discovery.
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