R-()-N-Benzyl-α-methylbenzylamine
97%
- Product Code: 56420
Alias:
(R)-(+)-N-Benzyl-1-phenylethylamine
CAS:
38235-77-7
| Molecular Weight: | 211.3 g./mol | Molecular Formula: | C₆H₅CHCH₃NHCH₂C₆H₅ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00015010 | |
| Melting Point: | Boiling Point: | 171 °C15 mm Hg(lit.) | |
| Density: | 1.01 g/mL at 25 °C(lit.) | Storage Condition: | room temperature |
Product Description:
This compound is widely utilized in the field of asymmetric synthesis, particularly as a chiral auxiliary or resolving agent. It plays a crucial role in the preparation of enantiomerically pure compounds, which are essential in the development of pharmaceuticals, agrochemicals, and fine chemicals. Its ability to induce chirality in reactions makes it valuable for creating specific stereoisomers with high precision. Additionally, it is employed in the synthesis of complex organic molecules, where controlling the stereochemistry is critical for achieving desired biological activity or material properties. Its application extends to catalysis, where it can be used to design chiral catalysts for enantioselective transformations.
Product Specification:
| Test | Specification |
|---|---|
| PurityGC | 96.5 100% |
| REFRACTIVE INDEX N20D | 1.562-1.564 |
| SPECIFIC GRAVITY 2020 | 1.009-1.011 |
| SPECIFIC ROTATIONA20DNEAT | 38-42 |
| APPEARANCE | Colorless to light yellow liquid |
| INFRARED SPECTRUM | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿300.00 |
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| 5.000 | 10-20 days | ฿490.00 |
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| 25.000 | 10-20 days | ฿1,300.00 |
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| 100.000 | 10-20 days | ฿3,220.00 |
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| 500.000 | 10-20 days | ฿14,200.00 |
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R-()-N-Benzyl-α-methylbenzylamine
This compound is widely utilized in the field of asymmetric synthesis, particularly as a chiral auxiliary or resolving agent. It plays a crucial role in the preparation of enantiomerically pure compounds, which are essential in the development of pharmaceuticals, agrochemicals, and fine chemicals. Its ability to induce chirality in reactions makes it valuable for creating specific stereoisomers with high precision. Additionally, it is employed in the synthesis of complex organic molecules, where controlling the stereochemistry is critical for achieving desired biological activity or material properties. Its application extends to catalysis, where it can be used to design chiral catalysts for enantioselective transformations.
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