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75968-40-0

(R)-4-CHLORO-ALPHA-METHYLBENZYL ALCOHOL

CAS: 75968-40-0

Molecular Formula: C8H9ClO

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75968-40-0 - Names and Identifiers

Name (R)-4-CHLORO-ALPHA-METHYLBENZYL ALCOHOL
Synonyms (R)-4-Chloro-1-phenylethanol
(R)-1-(4-Chlorophenyl)ethanol
(R)-1-(p-Chlorophenyl)ethanol
(1R)-1-(4-Chlorophenyl)ethanol
(R)-4-Chloro-α-methylbenzyl alcohol
(R)-α-Methyl-4-chlorobenzyl alcohol
(R)-4-Chloro-α-methylbenzyl alcohol
(R)-4-Chloro-α-methylbenzenemethanol
(αR)-α-Methyl-4-chlorobenzenemethanol
(R)-4-CHLORO-ALPHA-METHYLBENZYL ALCOHOL
CAS 75968-40-0

75968-40-0 - Physico-chemical Properties

Molecular FormulaC8H9ClO
Molar Mass156.61
Density1.158 g/mL at 25 °C
Boling Point240.6±15.0 °C(Predicted)
Specific Rotation(α)49 º (C=1.6 IN CHLOROFORM)
Flash Point110°C
pKa14.22±0.20(Predicted)
Storage Condition2-8°C
Refractive Indexn20/D 1.544
UseUses (R)-1-(4-chlorophenyl) ethanol was used as a research compound.

75968-40-0 - Risk and Safety

Hazard SymbolsXn - Harmful
Harmful
Risk CodesR22 - 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 DescriptionS26 - 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 Germany3

75968-40-0 - Nature

specific rotation 49 ° (C=1.6 IN CHLOROFORM)
optical activity (optical activity) [α]20/D 49.0°, c = 1.6 in chloroform
Last Update:2024-04-10 22:29:15

75968-40-0 - Synthesis

(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.

Last Update:2024-04-10 22:29:15

75968-40-0 - Reference Information

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.
Last Update:2024-04-09 20:52:54
75968-40-0
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