(S)-2-((tert-Butoxycarbonyl)amino)-2-(4-fluorophenyl)acetic acid
≥95%
- Product Code: 38079
CAS:
142186-36-5
| Molecular Weight: | 269.27 g./mol | Molecular Formula: | C₁₃H₁₆FNO₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD01320862 | |
| Melting Point: | Boiling Point: | 408.4°C at 760 mmHg | |
| Density: | Storage Condition: | 2-8°C, dry and sealed |
Product Description:
This compound is primarily utilized in the pharmaceutical industry as a key intermediate in the synthesis of various active pharmaceutical ingredients (APIs). It is particularly significant in the production of chiral drugs, where its stereochemistry plays a crucial role in ensuring the desired biological activity. The presence of the 4-fluorophenyl group enhances its application in the development of compounds with specific receptor-binding properties, often found in medications targeting neurological or cardiovascular conditions. Additionally, the tert-butoxycarbonyl (Boc) protecting group allows for selective reactions during multi-step synthetic processes, making it valuable for constructing complex molecules with precision. Its applications extend to research and development, where it is used to explore new therapeutic agents and optimize drug efficacy.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿2,556.00 |
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| 1.000 | 10-20 days | ฿6,399.00 |
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| 5.000 | 10-20 days | ฿19,242.00 |
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| 10.000 | 10-20 days | ฿31,410.00 |
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(S)-2-((tert-Butoxycarbonyl)amino)-2-(4-fluorophenyl)acetic acid
This compound is primarily utilized in the pharmaceutical industry as a key intermediate in the synthesis of various active pharmaceutical ingredients (APIs). It is particularly significant in the production of chiral drugs, where its stereochemistry plays a crucial role in ensuring the desired biological activity. The presence of the 4-fluorophenyl group enhances its application in the development of compounds with specific receptor-binding properties, often found in medications targeting neurological or cardiovascular conditions. Additionally, the tert-butoxycarbonyl (Boc) protecting group allows for selective reactions during multi-step synthetic processes, making it valuable for constructing complex molecules with precision. Its applications extend to research and development, where it is used to explore new therapeutic agents and optimize drug efficacy.
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