(R)-()-4-Methoxy-α-methylbenzylamine
98%
- Product Code: 71670
Alias:
(R)-(+)-1-(4-methoxyphenyl)ethylamine; (R)-(+)-1-(4-methoxyphenyl)ethylamine, (R)-p-methoxy phenylethylamine, (R)-(+)-4-methoxy-α-methylbenzylamine
CAS:
22038-86-4
| Molecular Weight: | 151.21 g./mol | Molecular Formula: | C₉H₁₃NO |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00671659 | |
| Melting Point: | Boiling Point: | 65°C 0,4mm | |
| Density: | 1.024 g/mL at 20 °C(lit.) | Storage Condition: | room temperature, sealed |
Product Description:
(R)-()-4-Methoxy-α-methylbenzylamine is primarily used as a chiral building block in the synthesis of various pharmaceuticals. Its chiral nature makes it valuable in the production of enantiomerically pure compounds, which are crucial for drugs that require specific stereochemistry to achieve desired biological activity. This compound is often employed in asymmetric synthesis, where it serves as a chiral auxiliary or ligand to induce stereoselectivity in chemical reactions. Additionally, it finds application in the development of agrochemicals and fine chemicals, where its structural framework contributes to the creation of biologically active molecules with enhanced efficacy and selectivity.
Product Specification:
| Test | Specification |
|---|---|
| PurityGC | 98 100% |
| SELECTIVE CHIRAL HPLC | 98-100 |
| SPECIFIC ROTATION A20DNEAT | 30-34 |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | $17.70 |
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| 5.000 | 10-20 days | $59.71 |
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| 25.000 | 10-20 days | $287.43 |
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(R)-()-4-Methoxy-α-methylbenzylamine
(R)-()-4-Methoxy-α-methylbenzylamine is primarily used as a chiral building block in the synthesis of various pharmaceuticals. Its chiral nature makes it valuable in the production of enantiomerically pure compounds, which are crucial for drugs that require specific stereochemistry to achieve desired biological activity. This compound is often employed in asymmetric synthesis, where it serves as a chiral auxiliary or ligand to induce stereoselectivity in chemical reactions. Additionally, it finds application in the development of agrochemicals and fine chemicals, where its structural framework contributes to the creation of biologically active molecules with enhanced efficacy and selectivity.
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