2-(tert-butoxycarbonyl)-2,3,4,5-tetrahydro-1H-pyrrolo[1,2-a][1,4]diazepine-4-carboxylic acid
≥95%
- Product Code: 62353
CAS:
1251017-62-5
| Molecular Weight: | 280.32 g./mol | Molecular Formula: | C₁₄H₂₀N₂O₄ |
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| EC Number: | MDL Number: | MFCD18792196 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, sealed, dry |
Product Description:
This compound is primarily utilized in the field of organic synthesis and pharmaceutical research. It serves as a key intermediate in the development of various biologically active molecules, particularly in the synthesis of heterocyclic compounds. Its structure is valuable for constructing complex frameworks found in many therapeutic agents, including potential drugs targeting neurological disorders and cardiovascular diseases. Additionally, it is employed in the preparation of peptidomimetics, which mimic the structure and function of peptides, aiding in the study of protein interactions and drug design. Its tert-butoxycarbonyl (Boc) protecting group makes it particularly useful in multi-step synthetic processes, ensuring selective reactivity and stability during chemical transformations.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.001 | 10-20 days | ฿4,437.00 |
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| 0.005 | 10-20 days | ฿7,578.00 |
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2-(tert-butoxycarbonyl)-2,3,4,5-tetrahydro-1H-pyrrolo[1,2-a][1,4]diazepine-4-carboxylic acid
This compound is primarily utilized in the field of organic synthesis and pharmaceutical research. It serves as a key intermediate in the development of various biologically active molecules, particularly in the synthesis of heterocyclic compounds. Its structure is valuable for constructing complex frameworks found in many therapeutic agents, including potential drugs targeting neurological disorders and cardiovascular diseases. Additionally, it is employed in the preparation of peptidomimetics, which mimic the structure and function of peptides, aiding in the study of protein interactions and drug design. Its tert-butoxycarbonyl (Boc) protecting group makes it particularly useful in multi-step synthetic processes, ensuring selective reactivity and stability during chemical transformations.
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