(R)-2-Amino-3-(5-bromothiophen-2-yl)propanoic acid
97%
- Product Code: 55620
CAS:
264903-54-0
| Molecular Weight: | 250.11 g./mol | Molecular Formula: | C₇H₈BrNO₂S |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD04117831 | |
| Melting Point: | Boiling Point: | 340.664°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 medicinal chemistry and drug development. It serves as a key intermediate in the synthesis of various biologically active molecules, particularly those targeting neurological disorders. Its structure, featuring a bromothiophene moiety, makes it valuable for creating compounds that interact with specific receptors in the brain, such as glutamate receptors, which are implicated in conditions like epilepsy and neurodegenerative diseases. Additionally, it is used in research to study the structure-activity relationships of amino acid derivatives, aiding in the design of more effective therapeutic agents. Its chiral nature also allows for the development of enantiomerically pure drugs, enhancing pharmacological efficacy and reducing side effects.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿432.00 |
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| 0.250 | 10-20 days | ฿720.00 |
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| 1.000 | 10-20 days | ฿2,178.00 |
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(R)-2-Amino-3-(5-bromothiophen-2-yl)propanoic acid
This compound is primarily utilized in the field of medicinal chemistry and drug development. It serves as a key intermediate in the synthesis of various biologically active molecules, particularly those targeting neurological disorders. Its structure, featuring a bromothiophene moiety, makes it valuable for creating compounds that interact with specific receptors in the brain, such as glutamate receptors, which are implicated in conditions like epilepsy and neurodegenerative diseases. Additionally, it is used in research to study the structure-activity relationships of amino acid derivatives, aiding in the design of more effective therapeutic agents. Its chiral nature also allows for the development of enantiomerically pure drugs, enhancing pharmacological efficacy and reducing side effects.
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