(R)-3-(Benzo[b]thiophen-3-yl)-2-((tert-butoxycarbonyl)amino)propanoic acid
≥95%
- Product Code: 53465
CAS:
111082-76-9
Molecular Weight: | 321.39 g./mol | Molecular Formula: | C₁₆H₁₉NO₄S |
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EC Number: | MDL Number: | MFCD00079679 | |
Melting Point: | Boiling Point: | 514.1°C at 760 mmHg | |
Density: | Storage Condition: | 2-8°C, protected from light, stored in an inert gas |
Product Description:
This compound is primarily utilized in the field of pharmaceutical research and development, particularly in the synthesis of biologically active molecules. It serves as a key intermediate in the production of compounds targeting neurological disorders, such as Alzheimer's disease and other cognitive impairments. Its structure, featuring a benzo[b]thiophene moiety, makes it valuable for designing drugs that interact with specific receptors in the brain. Additionally, it is employed in the creation of peptide-based therapeutics, where the tert-butoxycarbonyl (Boc) protecting group ensures selective reactions during synthesis. Its applications also extend to the study of enzyme inhibition and the development of novel inhibitors for therapeutic purposes.
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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1.000 | 10-20 days | ฿1,548.00 |
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5.000 | 10-20 days | ฿6,993.00 |
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10.000 | 10-20 days | ฿13,752.00 |
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25.000 | 10-20 days | ฿33,723.00 |
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(R)-3-(Benzo[b]thiophen-3-yl)-2-((tert-butoxycarbonyl)amino)propanoic acid
This compound is primarily utilized in the field of pharmaceutical research and development, particularly in the synthesis of biologically active molecules. It serves as a key intermediate in the production of compounds targeting neurological disorders, such as Alzheimer's disease and other cognitive impairments. Its structure, featuring a benzo[b]thiophene moiety, makes it valuable for designing drugs that interact with specific receptors in the brain. Additionally, it is employed in the creation of peptide-based therapeutics, where the tert-butoxycarbonyl (Boc) protecting group ensures selective reactions during synthesis. Its applications also extend to the study of enzyme inhibition and the development of novel inhibitors for therapeutic purposes.
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