(S)-3-((tert-Butoxycarbonyl)amino)-4-(thiophen-2-yl)butanoic acid
96%
- Product Code: 38380
CAS:
190190-47-7
| Molecular Weight: | 285.36 g./mol | Molecular Formula: | C₁₃H₁₉NO₄S |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD01861081 | |
| Melting Point: | Boiling Point: | 449.3°C at 760 mmHg | |
| Density: | Storage Condition: | 2-8°C, dry and sealed away from light |
Product Description:
This compound is primarily utilized in the synthesis of pharmaceutical intermediates, particularly in the development of active pharmaceutical ingredients (APIs) for therapeutic drugs. Its structure, featuring a tert-butoxycarbonyl (Boc) protecting group and a thiophene moiety, makes it valuable in peptide chemistry and drug design. It is often employed in the preparation of compounds targeting neurological disorders, cardiovascular diseases, or inflammation due to its ability to modulate biological pathways. Additionally, it serves as a key building block in medicinal chemistry research, enabling the creation of molecules with enhanced bioavailability and specificity for target receptors. Its application extends to the production of small molecule inhibitors and enzyme modulators, contributing to advancements in drug discovery and development.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 G | 10-20 days | ฿12,438.00 |
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| 0.100 G | 10-20 days | ฿3,312.00 |
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| 0.250 G | 10-20 days | ฿4,968.00 |
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(S)-3-((tert-Butoxycarbonyl)amino)-4-(thiophen-2-yl)butanoic acid
This compound is primarily utilized in the synthesis of pharmaceutical intermediates, particularly in the development of active pharmaceutical ingredients (APIs) for therapeutic drugs. Its structure, featuring a tert-butoxycarbonyl (Boc) protecting group and a thiophene moiety, makes it valuable in peptide chemistry and drug design. It is often employed in the preparation of compounds targeting neurological disorders, cardiovascular diseases, or inflammation due to its ability to modulate biological pathways. Additionally, it serves as a key building block in medicinal chemistry research, enabling the creation of molecules with enhanced bioavailability and specificity for target receptors. Its application extends to the production of small molecule inhibitors and enzyme modulators, contributing to advancements in drug discovery and development.
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