(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
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
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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