6-oxaspiro[2.5]octan-1-ylmethanamine hydrochloride
95%
- Product Code: 75667
CAS:
1384431-19-9
| Molecular Weight: | 177.67 g./mol | Molecular Formula: | C₈H₁₆ClNO |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD22369951 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8℃ |
Product Description:
This compound is primarily utilized in the field of organic synthesis and medicinal chemistry. It serves as a key intermediate in the development of various pharmaceutical agents, particularly in the synthesis of complex molecules with potential therapeutic applications. Its spirocyclic structure makes it valuable for creating novel compounds with unique biological activities. Researchers often employ it in the design of drugs targeting neurological disorders, as its structural features can interact with specific receptors in the brain. Additionally, it is used in the preparation of specialized chemicals for research purposes, aiding in the exploration of new drug candidates and biochemical pathways. Its hydrochloride form enhances solubility, making it more suitable for use in aqueous-based reactions and formulations.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.010 | 10-20 days | ฿7,893.00 |
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| 0.050 | 10-20 days | ฿28,962.00 |
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6-oxaspiro[2.5]octan-1-ylmethanamine hydrochloride
This compound is primarily utilized in the field of organic synthesis and medicinal chemistry. It serves as a key intermediate in the development of various pharmaceutical agents, particularly in the synthesis of complex molecules with potential therapeutic applications. Its spirocyclic structure makes it valuable for creating novel compounds with unique biological activities. Researchers often employ it in the design of drugs targeting neurological disorders, as its structural features can interact with specific receptors in the brain. Additionally, it is used in the preparation of specialized chemicals for research purposes, aiding in the exploration of new drug candidates and biochemical pathways. Its hydrochloride form enhances solubility, making it more suitable for use in aqueous-based reactions and formulations.
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