5,6,7,8-Tetrahydro-1,8-naphthyridine-2-methanamine
95%
- Product Code: 72468
CAS:
332883-10-0
Molecular Weight: | 163.22 g./mol | Molecular Formula: | C₉H₁₃N₃ |
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EC Number: | MDL Number: | ||
Melting Point: | Boiling Point: | 336.9°C | |
Density: | Storage Condition: | 2-8°C |
Product Description:
This compound is primarily utilized in pharmaceutical research and development, particularly in the synthesis of novel drug candidates. It serves as a key intermediate in the creation of molecules targeting various therapeutic areas, including central nervous system disorders, due to its structural similarity to biologically active amines. Its naphthyridine core is often exploited for its ability to interact with enzymes and receptors, making it valuable in designing inhibitors or modulators for specific biological pathways. Additionally, it has potential applications in the development of anti-inflammatory and antimicrobial agents, as its scaffold can be modified to enhance binding affinity and selectivity. Researchers also explore its use in organic synthesis to construct complex heterocyclic compounds with potential pharmacological activity.
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.025 | 10-20 days | $169.54 |
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0.100 | 10-20 days | $356.93 |
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5,6,7,8-Tetrahydro-1,8-naphthyridine-2-methanamine
This compound is primarily utilized in pharmaceutical research and development, particularly in the synthesis of novel drug candidates. It serves as a key intermediate in the creation of molecules targeting various therapeutic areas, including central nervous system disorders, due to its structural similarity to biologically active amines. Its naphthyridine core is often exploited for its ability to interact with enzymes and receptors, making it valuable in designing inhibitors or modulators for specific biological pathways. Additionally, it has potential applications in the development of anti-inflammatory and antimicrobial agents, as its scaffold can be modified to enhance binding affinity and selectivity. Researchers also explore its use in organic synthesis to construct complex heterocyclic compounds with potential pharmacological activity.
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