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Rac-1-(1-phenylcyclohexyl)ethan-1-ol is a chiral organic compound with the molecular formula C15H22O. It is a racemate, meaning it consists of equal amounts of both R and S enantiomers. rac-1-(1-phenylcyclohexyl)ethan-1-ol features a cyclohexane ring with a phenyl group attached to one carbon and an ethanol group attached to the adjacent carbon. Rac-1-(1-phenylcyclohexyl)ethan-1-ol is an important intermediate in the synthesis of various pharmaceuticals and agrochemicals, particularly in the production of certain drugs that target the central nervous system. Its unique structure allows for the exploration of stereochemistry in drug design, potentially leading to more effective and selective medications.

6555-65-3

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6555-65-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6555-65-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,5,5 and 5 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 6555-65:
(6*6)+(5*5)+(4*5)+(3*5)+(2*6)+(1*5)=113
113 % 10 = 3
So 6555-65-3 is a valid CAS Registry Number.

6555-65-3Relevant academic research and scientific papers

Kinetic Resolution of Neopentylic Secondary Alcohols by Cu-H-Catalyzed Enantioselective Silylation with Hydrosilanes

Oestreich, Martin,Papadopulu, Zaneta

, p. 438 - 441 (2021/01/13)

A nonenzymatic kinetic resolution of sterically congested alcohols having a quaternary carbon atom in the β-position is reported. The catalyst system CuCl/NaOtBu/(R,R)-Ph-BPE together with a 3,5-xylyl-substituted tertiary hydrosilane enable enantioselective silylation of the hydroxy group. Several alcohols are obtained with good to excellent selectivity factors, and there are no other known straightforward methods to access these motifs.

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