(S)-(-)-1-Phenyl-1-propanol
98%
- Product Code: 74270
CAS:
613-87-6
| Molecular Weight: | 136.19 g./mol | Molecular Formula: | C₉H₁₂O |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00066207 | |
| Melting Point: | Boiling Point: | 94-95°C 10mm Hg (Lit.) | |
| Density: | 0.992 g/mL at 25 °C (lit.) | Storage Condition: | Room temperature, sealed, dry |
Product Description:
(S)-(-)-1-Phenyl-1-propanol is widely used in the synthesis of chiral compounds, particularly in the pharmaceutical industry, where it serves as a key intermediate for producing enantiomerically pure drugs. Its chiral nature makes it valuable in asymmetric synthesis, enabling the creation of specific stereoisomers that are often required for active pharmaceutical ingredients. Additionally, it is utilized in the preparation of fragrances and flavoring agents, contributing to the development of complex aromatic profiles. In research, it is employed as a building block for studying stereochemistry and developing new catalytic processes. Its applications also extend to agrochemicals, where it aids in the production of chiral pesticides and herbicides.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | Colorless to YellowLiquid |
| PURITY | 97.5-100 |
| Infrared spectrum | Conforms to Structure |
| NMR | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.050 | 10-20 days | ฿1,380.00 |
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(S)-(-)-1-Phenyl-1-propanol
(S)-(-)-1-Phenyl-1-propanol is widely used in the synthesis of chiral compounds, particularly in the pharmaceutical industry, where it serves as a key intermediate for producing enantiomerically pure drugs. Its chiral nature makes it valuable in asymmetric synthesis, enabling the creation of specific stereoisomers that are often required for active pharmaceutical ingredients. Additionally, it is utilized in the preparation of fragrances and flavoring agents, contributing to the development of complex aromatic profiles. In research, it is employed as a building block for studying stereochemistry and developing new catalytic processes. Its applications also extend to agrochemicals, where it aids in the production of chiral pesticides and herbicides.
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