(R)-()-1-Phenyl-1-propanol
99%
- Product Code: 74249
CAS:
1565-74-8
| Molecular Weight: | 136.19 g./mol | Molecular Formula: | C₉H₁₂O |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00064279 | |
| Melting Point: | Boiling Point: | 218-220°C (Lit.) | |
| Density: | 0.993 g/mL at 20 °C (lit.) | Storage Condition: | Room temperature, sealed, dry |
Product Description:
(R)-()-1-Phenyl-1-propanol is primarily used as a chiral intermediate in the synthesis of various pharmaceuticals and fine chemicals. Its enantiomeric purity makes it valuable in the production of optically active compounds, particularly in the development of drugs where stereochemistry plays a critical role in efficacy and safety. This compound is often employed in asymmetric synthesis and catalytic processes to create complex molecules with high enantioselectivity. Additionally, it serves as a building block in the preparation of agrochemicals, fragrances, and specialty chemicals, where its specific stereochemistry enhances the desired properties of the final product. Its application extends to research and development in organic chemistry, particularly in studies focusing on chiral resolution and enantioselective reactions.
Product Specification:
| Test | Specification |
|---|---|
| Purity | 98.5 100% |
| SPECIFIC ROTATION A20DC1 CHCL3 | 44 47 |
| REFRACTIVE INDEX N20D | 1.518-1.522 |
| Appearance | Colorless to light yellow liquid |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | €303.39 |
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(R)-()-1-Phenyl-1-propanol
(R)-()-1-Phenyl-1-propanol is primarily used as a chiral intermediate in the synthesis of various pharmaceuticals and fine chemicals. Its enantiomeric purity makes it valuable in the production of optically active compounds, particularly in the development of drugs where stereochemistry plays a critical role in efficacy and safety. This compound is often employed in asymmetric synthesis and catalytic processes to create complex molecules with high enantioselectivity. Additionally, it serves as a building block in the preparation of agrochemicals, fragrances, and specialty chemicals, where its specific stereochemistry enhances the desired properties of the final product. Its application extends to research and development in organic chemistry, particularly in studies focusing on chiral resolution and enantioselective reactions.
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