3-[3-(Trifluoromethyl)phenoxy]-azetidine hydrochloride
97%
- Product Code: 117584
CAS:
1188374-88-0
| Molecular Weight: | 253.65 g./mol | Molecular Formula: | C₁₀H₁₁ClF₃NO |
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| EC Number: | MDL Number: | MFCD05664837 | |
| Melting Point: | Boiling Point: | ||
| 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. Its structure, featuring a trifluoromethylphenoxy group and an azetidine ring, makes it a valuable intermediate for designing molecules with potential therapeutic properties. It is often explored in the development of central nervous system (CNS) drugs, as the azetidine moiety can enhance blood-brain barrier penetration. Additionally, the trifluoromethyl group contributes to metabolic stability and binding affinity, making it useful in optimizing pharmacokinetic properties. Researchers also investigate its role in creating anti-inflammatory, analgesic, or antimicrobial agents, leveraging its unique chemical framework to target specific biological pathways.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.050 | 10-20 days | $54.82 |
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| 0.250 | 10-20 days | $166.95 |
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3-[3-(Trifluoromethyl)phenoxy]-azetidine hydrochloride
This compound is primarily utilized in pharmaceutical research and development, particularly in the synthesis of novel drug candidates. Its structure, featuring a trifluoromethylphenoxy group and an azetidine ring, makes it a valuable intermediate for designing molecules with potential therapeutic properties. It is often explored in the development of central nervous system (CNS) drugs, as the azetidine moiety can enhance blood-brain barrier penetration. Additionally, the trifluoromethyl group contributes to metabolic stability and binding affinity, making it useful in optimizing pharmacokinetic properties. Researchers also investigate its role in creating anti-inflammatory, analgesic, or antimicrobial agents, leveraging its unique chemical framework to target specific biological pathways.
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