Benzyl 4-Nitroazepane-1-Carboxylate
95%
- Product Code: 123158
CAS:
1823863-01-9
Molecular Weight: | 278.3 g./mol | Molecular Formula: | C₁₄H₁₈N₂O₄ |
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EC Number: | MDL Number: | MFCD27997474 | |
Melting Point: | Boiling Point: | ||
Density: | Storage Condition: | 2-8°C, dry, sealed |
Product Description:
Benzyl 4-Nitroazepane-1-Carboxylate is primarily utilized in organic synthesis as an intermediate for the development of more complex chemical compounds. Its structure, featuring both a nitro group and a benzyl ester, makes it a versatile building block in pharmaceutical research, particularly in the synthesis of nitrogen-containing heterocycles. These heterocycles are often explored for their potential biological activities, including antimicrobial, anticancer, and central nervous system-targeting properties. Additionally, the compound’s reactive sites allow for further functionalization, enabling researchers to tailor its properties for specific applications in drug discovery and medicinal chemistry. Its use is also seen in the preparation of peptidomimetics, which are compounds designed to mimic peptides for therapeutic purposes.
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.250 | 10-20 days | $490.37 |
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1.000 | 10-20 days | $1,031.50 |
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Benzyl 4-Nitroazepane-1-Carboxylate
Benzyl 4-Nitroazepane-1-Carboxylate is primarily utilized in organic synthesis as an intermediate for the development of more complex chemical compounds. Its structure, featuring both a nitro group and a benzyl ester, makes it a versatile building block in pharmaceutical research, particularly in the synthesis of nitrogen-containing heterocycles. These heterocycles are often explored for their potential biological activities, including antimicrobial, anticancer, and central nervous system-targeting properties. Additionally, the compound’s reactive sites allow for further functionalization, enabling researchers to tailor its properties for specific applications in drug discovery and medicinal chemistry. Its use is also seen in the preparation of peptidomimetics, which are compounds designed to mimic peptides for therapeutic purposes.
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