3-((tert-Butoxycarbonyl)amino)-3-(4-fluorophenyl)propanoic acid
97%
- Product Code: 117480
CAS:
284493-72-7
| Molecular Weight: | 283.30 g./mol | Molecular Formula: | C₁₄H₁₈FNO₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD02090715 | |
| Melting Point: | Boiling Point: | 424.5°C at 760 mmHg | |
| Density: | Storage Condition: | 2-8°C, dry and sealed |
Product Description:
This compound is primarily utilized in the pharmaceutical and organic synthesis industries as a key intermediate in the production of more complex molecules. It is often employed in the development of active pharmaceutical ingredients (APIs), particularly those targeting neurological or psychiatric conditions, due to the presence of the fluorophenyl group, which can enhance binding affinity and metabolic stability. Additionally, the tert-butoxycarbonyl (Boc) protecting group in its structure makes it valuable in peptide synthesis, where it safeguards the amino group during reactions, allowing for selective deprotection and further functionalization. Its application extends to research settings for studying enzyme interactions and drug metabolism, owing to its structural versatility and potential bioactive properties.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿999.00 |
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| 1.000 | 10-20 days | ฿2,493.00 |
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| 5.000 | 10-20 days | ฿7,533.00 |
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| 10.000 | 10-20 days | ฿12,573.00 |
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3-((tert-Butoxycarbonyl)amino)-3-(4-fluorophenyl)propanoic acid
This compound is primarily utilized in the pharmaceutical and organic synthesis industries as a key intermediate in the production of more complex molecules. It is often employed in the development of active pharmaceutical ingredients (APIs), particularly those targeting neurological or psychiatric conditions, due to the presence of the fluorophenyl group, which can enhance binding affinity and metabolic stability. Additionally, the tert-butoxycarbonyl (Boc) protecting group in its structure makes it valuable in peptide synthesis, where it safeguards the amino group during reactions, allowing for selective deprotection and further functionalization. Its application extends to research settings for studying enzyme interactions and drug metabolism, owing to its structural versatility and potential bioactive properties.
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