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1-(1-methylcyclohexyl)ethan-1-ol, also known as 1-methyl-1-cyclohexylethanol or methylcyclohexyl carbinol, is an organic compound with the molecular formula C9H18O. It is a colorless liquid with a camphoraceous odor and is used as a fragrance ingredient in various applications, including perfumes, cosmetics, and household products. 1-(1-methylcyclohexyl)ethan-1-ol is characterized by its unique structure, featuring a cyclohexane ring with a methyl group attached to one carbon and an ethyl group attached to the adjacent carbon, with a hydroxyl group on the terminal carbon of the ethyl chain. It is synthesized through various chemical reactions, such as the reduction of 1-methylcyclohexanone or the addition of ethylmagnesium bromide to cyclohexanone. Due to its versatile chemical properties, 1-(1-methylcyclohexyl)ethan-1-ol is an important intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other specialty chemicals.

6555-61-9

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6555-61-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6555-61-9 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 1 respectively.
Calculate Digit Verification of CAS Registry Number 6555-61:
(6*6)+(5*5)+(4*5)+(3*5)+(2*6)+(1*1)=109
109 % 10 = 9
So 6555-61-9 is a valid CAS Registry Number.

6555-61-9Relevant academic research and scientific papers

Enantioconvergent alkylation of ketones with racemic secondary alcohols: Via hydrogen borrowing catalysis

Cheang, Daniella M. J.,Armstrong, Roly J.,Akhtar, Wasim M.,Donohoe, Timothy J.

supporting information, p. 3543 - 3546 (2020/04/03)

An enantioconvergent method for the alkylation of o-disubstituted aryl ketones with racemic secondary alcohols is described. This process is mediated by a commercially available iridium catalyst and proceeds via hydrogen borrowing catalysis. The highly enantioenriched β-substituted ketone products were readily cleaved to a wide range of functional groups via retro-Friedel-Crafts acylation.

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