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α-Isopropylcyclohexaneacetic acid is a complex organic compound with the molecular formula C??H??O?. It is a derivative of cyclohexane, featuring an isopropyl group (C?H?) attached to the cyclohexane ring and a carboxylic acid (COOH) functional group. This molecule is characterized by its unique structure, which combines the properties of a cycloalkane with those of a carboxylic acid. It is a white crystalline solid with a melting point of approximately 90°C. Due to its chemical structure, α-isopropylcyclohexaneacetic acid has potential applications in the synthesis of pharmaceuticals and other organic compounds, as well as in the field of materials science.

19986-15-3

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19986-15-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 19986-15-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,9,8 and 6 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 19986-15:
(7*1)+(6*9)+(5*9)+(4*8)+(3*6)+(2*1)+(1*5)=163
163 % 10 = 3
So 19986-15-3 is a valid CAS Registry Number.

19986-15-3Downstream Products

19986-15-3Relevant academic research and scientific papers

Enantioselective synthesis of allenecarboxylates from phenyl acetates through C-C bond forming reactions

Yamazaki, Jiro,Watanabe, Toshiyuki,Tanaka, Kiyoshi

, p. 669 - 675 (2007/10/03)

A variety of optically active 4,4-disubstituted allenecarboxylic acid methyl esters were prepared from simple α,α-disubstituted phenyl acetate through base treatment of the esters to generate ketenes, followed by successive Horner-Wadsworth-Emmons reaction. The transformation was further developed as a one-pot procedure with satisfactory yields and high enantioselectivity.

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