(1R,2S)-rel-Methyl 2-((tert-butoxycarbonyl)amino)cyclopropanecarboxylate
98%
- Product Code: 36215
CAS:
170299-60-2
| Molecular Weight: | 215.2500 g./mol | Molecular Formula: | C₁₀H₁₇NO₄ |
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| EC Number: | MDL Number: | MFCD28501607 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature |
Product Description:
This compound is primarily used in organic synthesis and pharmaceutical research as a key intermediate in the preparation of more complex molecules. Its structure, featuring a cyclopropane ring and a tert-butoxycarbonyl (Boc) protecting group, makes it valuable for constructing biologically active compounds, particularly in the development of drugs targeting neurological disorders or as a building block for peptidomimetics. The Boc group can be easily removed under mild acidic conditions, allowing for further functionalization of the molecule. Additionally, the cyclopropane ring imparts rigidity and stability, which is advantageous in designing molecules with specific conformational properties. Its applications extend to the synthesis of chiral compounds, where the stereochemistry of the molecule plays a critical role in its biological activity.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿6,021.00 |
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(1R,2S)-rel-Methyl 2-((tert-butoxycarbonyl)amino)cyclopropanecarboxylate
This compound is primarily used in organic synthesis and pharmaceutical research as a key intermediate in the preparation of more complex molecules. Its structure, featuring a cyclopropane ring and a tert-butoxycarbonyl (Boc) protecting group, makes it valuable for constructing biologically active compounds, particularly in the development of drugs targeting neurological disorders or as a building block for peptidomimetics. The Boc group can be easily removed under mild acidic conditions, allowing for further functionalization of the molecule. Additionally, the cyclopropane ring imparts rigidity and stability, which is advantageous in designing molecules with specific conformational properties. Its applications extend to the synthesis of chiral compounds, where the stereochemistry of the molecule plays a critical role in its biological activity.
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