Molecular Formula | C8H9ClO |
Molar Mass | 156.61 |
Density | 1.158 g/mL at 25 °C |
Boling Point | 240.6±15.0 °C(Predicted) |
Specific Rotation(α) | 49 º (C=1.6 IN CHLOROFORM) |
Flash Point | 110°C |
pKa | 14.22±0.20(Predicted) |
Storage Condition | 2-8°C |
Refractive Index | n20/D 1.544 |
Use | Uses (R)-1-(4-chlorophenyl) ethanol was used as a research compound. |
Hazard Symbols | Xn - Harmful |
Risk Codes | R22 - Harmful if swallowed R41 - Risk of serious damage to eyes R52/53 - Harmful to aquatic organisms, may cause long-term adverse effects in the aquatic environment. |
Safety Description | S26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice. S39 - Wear eye / face protection. S61 - Avoid release to the environment. Refer to special instructions / safety data sheets. |
WGK Germany | 3 |
specific rotation | 49 ° (C=1.6 IN CHLOROFORM) |
optical activity (optical activity) | [α]20/D 49.0°, c = 1.6 in chloroform |
(R)-1-(4-chlorophenyl) ethanol can be used for:
As a substrate in the racemization of secondary alcohols using ruthenium hydroxide complexes.
In the synthesis of 2,3,4, 9-tetrahydro-1H-carbazole as an effective DP1 antagonist.
As a substrate, chiral 3-aryl-3-substituted propionic acid is synthesized by Mitsunobu reaction.
use | (R)-1-(4-chlorophenyl) ethanol is used as a research compound. |
Synthesis | (R)-1-(4-chlorophenyl) ethanol can be used: as a substrate in the racemization process of secondary alcohols using ruthenium hydroxide complexes. In the synthesis of 2,3, 4,9-tetrahydro-1H-carbazole as a potent DP1 antagonist. As a substrate, chiral 3-aryl-3-substituted propionic acid is synthesized by Mitsunobu reaction. |