3-(5-bromothiophen-2-yl)-2-((tert-butoxycarbonyl)amino)propanoic acid
95%
- Product Code: 60708
CAS:
190319-95-0
| Molecular Weight: | 350.23 g./mol | Molecular Formula: | C₁₂H₁₆BrNO₄S |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD01320846 | |
| Melting Point: | Boiling Point: | 473.8±45.0 °C(Predicted) | |
| Density: | 1.494±0.06 g/cm3(Predicted) | Storage Condition: | 2-8°C, sealed, dry |
Product Description:
This compound is primarily utilized in organic synthesis and pharmaceutical research. It serves as a key intermediate in the development of peptidomimetics and bioactive molecules. The tert-butoxycarbonyl (Boc) protecting group allows for selective deprotection during multi-step synthesis, enabling the creation of complex structures. Its bromothiophene moiety is particularly valuable in designing compounds with potential therapeutic applications, such as enzyme inhibitors or receptor modulators. Additionally, it is employed in the study of structure-activity relationships (SAR) to optimize drug candidates for improved efficacy and selectivity.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿2,430.00 |
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| 0.250 | 10-20 days | ฿4,860.00 |
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| 1.000 | 10-20 days | ฿15,120.00 |
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3-(5-bromothiophen-2-yl)-2-((tert-butoxycarbonyl)amino)propanoic acid
This compound is primarily utilized in organic synthesis and pharmaceutical research. It serves as a key intermediate in the development of peptidomimetics and bioactive molecules. The tert-butoxycarbonyl (Boc) protecting group allows for selective deprotection during multi-step synthesis, enabling the creation of complex structures. Its bromothiophene moiety is particularly valuable in designing compounds with potential therapeutic applications, such as enzyme inhibitors or receptor modulators. Additionally, it is employed in the study of structure-activity relationships (SAR) to optimize drug candidates for improved efficacy and selectivity.
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