3-(1-((tert-Butoxycarbonyl)amino)ethyl)benzoic acid
90%
- Product Code: 44176
CAS:
165949-84-8
| Molecular Weight: | 265.3050 g./mol | Molecular Formula: | C₁₄H₁₉NO₄ |
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| EC Number: | MDL Number: | MFCD12913674 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature |
Product Description:
This chemical is primarily used as an intermediate in the synthesis of more complex organic compounds, particularly in pharmaceutical research and development. It is often employed in the preparation of active pharmaceutical ingredients (APIs) due to its functional groups, which allow for further chemical modifications. The tert-butoxycarbonyl (Boc) group serves as a protective group for amines, enabling selective reactions in multi-step synthetic processes. Its benzoic acid moiety also provides a versatile handle for coupling reactions, making it valuable in the creation of peptidomimetics, small molecule drugs, and other biologically active compounds. Additionally, it finds utility in the development of prodrugs and in medicinal chemistry for optimizing drug properties such as solubility, stability, and bioavailability.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿6,606.00 |
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3-(1-((tert-Butoxycarbonyl)amino)ethyl)benzoic acid
This chemical is primarily used as an intermediate in the synthesis of more complex organic compounds, particularly in pharmaceutical research and development. It is often employed in the preparation of active pharmaceutical ingredients (APIs) due to its functional groups, which allow for further chemical modifications. The tert-butoxycarbonyl (Boc) group serves as a protective group for amines, enabling selective reactions in multi-step synthetic processes. Its benzoic acid moiety also provides a versatile handle for coupling reactions, making it valuable in the creation of peptidomimetics, small molecule drugs, and other biologically active compounds. Additionally, it finds utility in the development of prodrugs and in medicinal chemistry for optimizing drug properties such as solubility, stability, and bioavailability.
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