2-Amino-3-(7-bromo-1H-indol-3-yl)propanoic acid
97%
- Product Code: 52216
CAS:
852391-45-8
| Molecular Weight: | 283.12 g./mol | Molecular Formula: | C₁₁H₁₁BrN₂O₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD04972047 | |
| Melting Point: | Boiling Point: | 495.849°C at 760 mmHg | |
| Density: | 1.705 g/cm3 | Storage Condition: | 2-8°C, dry and sealed away from light |
Product Description:
This compound is primarily utilized in biochemical research, particularly in studies involving the synthesis and modification of peptides and proteins. Its unique structure, which includes an indole moiety, makes it valuable for investigating enzyme-substrate interactions and receptor binding studies. Additionally, it serves as a building block in the development of novel pharmaceutical compounds, especially those targeting neurological disorders due to its potential to interact with neurotransmitter systems. Researchers also explore its use in fluorescence labeling and imaging techniques, leveraging its bromine atom for further functionalization.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | White to yellow powder or crystals |
| PURITY | 96.5-100 |
| Infrared spectrum | Conforms to Structure |
| NMR | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿6,470.00 |
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| 0.250 | 10-20 days | ฿9,690.00 |
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| 1.000 | 10-20 days | ฿24,220.00 |
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2-Amino-3-(7-bromo-1H-indol-3-yl)propanoic acid
This compound is primarily utilized in biochemical research, particularly in studies involving the synthesis and modification of peptides and proteins. Its unique structure, which includes an indole moiety, makes it valuable for investigating enzyme-substrate interactions and receptor binding studies. Additionally, it serves as a building block in the development of novel pharmaceutical compounds, especially those targeting neurological disorders due to its potential to interact with neurotransmitter systems. Researchers also explore its use in fluorescence labeling and imaging techniques, leveraging its bromine atom for further functionalization.
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