Methyl 3-(1-((tert-butoxycarbonyl)amino)ethyl)benzoate
95%
- Product Code: 44177
CAS:
1027256-76-3
| Molecular Weight: | 279.3315 g./mol | Molecular Formula: | C₁₅H₂₁NO₄ |
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| EC Number: | MDL Number: | MFCD28403457 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature |
Product Description:
This compound is primarily utilized in organic synthesis as an intermediate for the preparation of more complex molecules. It is often employed in the pharmaceutical industry for the development of active pharmaceutical ingredients (APIs), particularly in the synthesis of compounds with potential therapeutic properties. The tert-butoxycarbonyl (Boc) protecting group in the molecule is crucial for safeguarding the amine functionality during multi-step synthetic processes, allowing for selective reactions to occur at other sites. Additionally, it finds application in the research and development of peptidomimetics and other bioactive molecules where controlled deprotection of the amine group is required. Its role in facilitating the synthesis of structurally diverse compounds makes it valuable in medicinal chemistry and drug discovery.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿9,279.00 |
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Methyl 3-(1-((tert-butoxycarbonyl)amino)ethyl)benzoate
This compound is primarily utilized in organic synthesis as an intermediate for the preparation of more complex molecules. It is often employed in the pharmaceutical industry for the development of active pharmaceutical ingredients (APIs), particularly in the synthesis of compounds with potential therapeutic properties. The tert-butoxycarbonyl (Boc) protecting group in the molecule is crucial for safeguarding the amine functionality during multi-step synthetic processes, allowing for selective reactions to occur at other sites. Additionally, it finds application in the research and development of peptidomimetics and other bioactive molecules where controlled deprotection of the amine group is required. Its role in facilitating the synthesis of structurally diverse compounds makes it valuable in medicinal chemistry and drug discovery.
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