(R)-()-α−Methyl-1-naphthalenemethanol
99%
- Product Code: 76916
CAS:
42177-25-3
| Molecular Weight: | 172.22 g./mol | Molecular Formula: | C₁₀H₇CHCH₃OH |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00077830 | |
| Melting Point: | 47°C - 49°C | Boiling Point: | |
| Density: | Storage Condition: | room temperature |
Product Description:
This chemical is widely used as a chiral resolving agent in the separation of enantiomers, particularly in the pharmaceutical industry. It is employed to resolve racemic mixtures, enabling the isolation of specific enantiomers that may have distinct biological activities. Additionally, it serves as a key intermediate in the synthesis of optically active compounds, contributing to the production of drugs and fine chemicals with high enantiomeric purity. Its application extends to asymmetric synthesis, where it acts as a chiral auxiliary or catalyst, enhancing the stereoselectivity of chemical reactions.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | Colorless to Light Yellow Viscous Liquid or Solid |
| PURITY | 98.5-100 |
| Infrared spectrum | Conforms to Structure |
| NMR | Conforms to Structure |
| NOTE: | This product is low melting point solid,may change state in different environments (solid, liquid or semi-solid) |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | €485.69 |
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| 1.000 | 10-20 days | €1,318.84 |
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(R)-()-α−Methyl-1-naphthalenemethanol
This chemical is widely used as a chiral resolving agent in the separation of enantiomers, particularly in the pharmaceutical industry. It is employed to resolve racemic mixtures, enabling the isolation of specific enantiomers that may have distinct biological activities. Additionally, it serves as a key intermediate in the synthesis of optically active compounds, contributing to the production of drugs and fine chemicals with high enantiomeric purity. Its application extends to asymmetric synthesis, where it acts as a chiral auxiliary or catalyst, enhancing the stereoselectivity of chemical reactions.
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