101266-82-4 Usage
Description
1-(1-phenyl-cyclopentyl)-ethanol is a chemical compound with the molecular formula C14H18O, featuring a phenyl group and a cyclopentyl group attached to an ethanol molecule. It is an organic compound that is commonly utilized in the synthesis of pharmaceuticals and other organic compounds. Due to its unique structure, it may exhibit specific chemical and physical properties, making it a valuable compound for various applications in the fields of chemical and pharmaceutical research.
Uses
Used in Pharmaceutical Synthesis:
1-(1-phenyl-cyclopentyl)-ethanol is used as a key intermediate for the synthesis of various pharmaceuticals. Its unique structure allows for the creation of complex molecules that can be used in the development of new drugs.
Used in Organic Chemistry:
In the field of organic chemistry, 1-(1-phenyl-cyclopentyl)-ethanol serves as a reagent or intermediate for the production of complex molecules. Its specific chemical and physical properties make it a useful compound for research and development in this area.
Used in Chemical Research:
1-(1-phenyl-cyclopentyl)-ethanol is also utilized in chemical research to study its properties and potential applications. Its unique structure and the presence of both a phenyl group and a cyclopentyl group attached to an ethanol molecule make it an interesting subject for further investigation and potential use in various chemical processes.
Check Digit Verification of cas no
The CAS Registry Mumber 101266-82-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,1,2,6 and 6 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 101266-82:
(8*1)+(7*0)+(6*1)+(5*2)+(4*6)+(3*6)+(2*8)+(1*2)=84
84 % 10 = 4
So 101266-82-4 is a valid CAS Registry Number.
101266-82-4Relevant articles and documents
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.
