(S)-2-Amino-3-(benzo[b]thiophen-3-yl)propanoic acid
97%
- Product Code: 53459
CAS:
72120-71-9
Molecular Weight: | 221.28 g./mol | Molecular Formula: | C₁₁H₁₁NO₂S |
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EC Number: | MDL Number: | MFCD00079684 | |
Melting Point: | Boiling Point: | 416.7°C at 760 mmHg | |
Density: | Storage Condition: | 2-8°C, protected from light, stored in an inert gas |
Product Description:
This compound is primarily used in the field of medicinal chemistry and drug development. It serves as a key intermediate in the synthesis of various pharmaceutical agents, particularly those targeting neurological and psychiatric disorders. Its structure, which includes a benzo[b]thiophene moiety, makes it valuable for designing molecules that interact with specific receptors in the brain, such as serotonin or dopamine receptors. Researchers utilize it to develop potential treatments for conditions like depression, schizophrenia, and Parkinson's disease. Additionally, its chiral nature allows for the creation of enantiomerically pure compounds, enhancing the specificity and efficacy of the resulting drugs.
Product Specification:
Test | Specification |
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APPEARANCE | solid |
PURITY | 96.5-100 |
Infrared spectrum | Conforms to Structure |
NMR | Conforms to Structure |
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.250 | 10-20 days | ฿2,260.00 |
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1.000 | 10-20 days | ฿6,900.00 |
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5.000 | 10-20 days | ฿28,760.00 |
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(S)-2-Amino-3-(benzo[b]thiophen-3-yl)propanoic acid
This compound is primarily used in the field of medicinal chemistry and drug development. It serves as a key intermediate in the synthesis of various pharmaceutical agents, particularly those targeting neurological and psychiatric disorders. Its structure, which includes a benzo[b]thiophene moiety, makes it valuable for designing molecules that interact with specific receptors in the brain, such as serotonin or dopamine receptors. Researchers utilize it to develop potential treatments for conditions like depression, schizophrenia, and Parkinson's disease. Additionally, its chiral nature allows for the creation of enantiomerically pure compounds, enhancing the specificity and efficacy of the resulting drugs.
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