N-Boc-2-(4-Aminophenyl)ethanol
98%
- Product Code: 61075
CAS:
104060-23-3
| Molecular Weight: | 237.3 g./mol | Molecular Formula: | C₁₃H₁₉NO₃ |
|---|---|---|---|
| EC Number: | MDL Number: | ||
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature, dry |
Product Description:
N-Boc-2-(4-Aminophenyl)ethanol is widely used in organic synthesis as a key intermediate for the preparation of pharmaceuticals and bioactive compounds. Its primary application lies in the synthesis of various drugs, particularly those targeting the central nervous system, due to the presence of the protected amino group. The Boc group serves as a protective moiety, allowing selective reactions to occur at other functional sites in the molecule. It is also utilized in the development of peptidomimetics and other biologically active molecules, where the 4-aminophenyl moiety can be further modified to enhance binding affinity or pharmacological properties. Additionally, this compound is employed in the synthesis of complex organic molecules for research purposes, particularly in medicinal chemistry and drug discovery. Its versatility and stability make it a valuable building block in multi-step synthetic pathways.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | White to off-white Solid |
| PURITY | 97.5-100 |
| Infrared spectrum | Conforms to Structure |
| NMR | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿630.00 |
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| 1.000 | 10-20 days | ฿1,610.00 |
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| 5.000 | 10-20 days | ฿5,650.00 |
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N-Boc-2-(4-Aminophenyl)ethanol
N-Boc-2-(4-Aminophenyl)ethanol is widely used in organic synthesis as a key intermediate for the preparation of pharmaceuticals and bioactive compounds. Its primary application lies in the synthesis of various drugs, particularly those targeting the central nervous system, due to the presence of the protected amino group. The Boc group serves as a protective moiety, allowing selective reactions to occur at other functional sites in the molecule. It is also utilized in the development of peptidomimetics and other biologically active molecules, where the 4-aminophenyl moiety can be further modified to enhance binding affinity or pharmacological properties. Additionally, this compound is employed in the synthesis of complex organic molecules for research purposes, particularly in medicinal chemistry and drug discovery. Its versatility and stability make it a valuable building block in multi-step synthetic pathways.
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