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(1Ξ,4R)-2-oxo-4-methyl-cyclohexanecarboxylic acid ethyl ester is a complex organic compound with the molecular formula C11H18O3. It is a derivative of cyclohexanecarboxylic acid, featuring a methyl group at the 4-position and an oxo group at the 2-position. The ethyl ester functional group is attached to the carboxylic acid, which is characteristic of esters. (1Ξ,4R)-2-oxo-4-methyl-cyclohexanecarboxylic acid ethyl ester is known for its potential applications in the synthesis of various pharmaceuticals and agrochemicals due to its unique structure and reactivity. It is a chiral molecule, with the 1-position being in the equatorial (Ξ) configuration and the 4-position in the right-handed (R) configuration, which can influence its biological activity and stereoselective reactions.

13368-67-7

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13368-67-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 13368-67-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,3,6 and 8 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 13368-67:
(7*1)+(6*3)+(5*3)+(4*6)+(3*8)+(2*6)+(1*7)=107
107 % 10 = 7
So 13368-67-7 is a valid CAS Registry Number.

13368-67-7Relevant academic research and scientific papers

An enantiodivergent formal synthesis of paecilomycine A

Mehta, Goverdhan,Samineni, Ramesh,Srihari, Pabbaraja

scheme or table, p. 829 - 832 (2012/03/09)

A concise, enantiodivergent formal synthesis of (+)-paecilomycine A and its antipode, involving a 1,4-chirality transfer protocol and an intramolecular Pauson-Khand reaction as the key steps is outlined.

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