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Trans-1-Ethyl-4-tert-butyl-cyclohexan is a cyclic hydrocarbon compound with the molecular formula C12H24. It consists of a cyclohexane ring with an ethyl group attached to carbon 1 and a tert-butyl group attached to carbon 4. The "trans" configuration indicates that the ethyl and tert-butyl groups are positioned on opposite sides of the cyclohexane ring. trans-1-Ethyl-4-tert.-butyl-cyclohexan is an example of a disubstituted cycloalkane, which is a type of alkane with a ring structure. It is an organic compound that can be used in various chemical reactions and as a building block for more complex molecules. Due to its specific structure, it may have unique physical and chemical properties compared to other cycloalkanes, making it potentially useful in specific applications within the chemical industry.

1129-23-3

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1129-23-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1129-23-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,1,2 and 9 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1129-23:
(6*1)+(5*1)+(4*2)+(3*9)+(2*2)+(1*3)=53
53 % 10 = 3
So 1129-23-3 is a valid CAS Registry Number.

1129-23-3Downstream Products

1129-23-3Relevant academic research and scientific papers

Diastercoselectivity in the heterogeneous hydrogenation reactions of phosphorous substituted olefins

Huff, Bret E.,Khau, Vien V.,LeTourneau, Michael E.,Martinelli, Michael J.,Nayyar, Naresh K.,Peterson, Barry C.

, p. 8627 - 8630 (2007/10/03)

Phosphorous substituted methylenecyclohexane olefins show enhanced diastereoselectivity in heterogeneous hydrogenation reactions using Pd/C. A model system derived from 4-t-butylcyclohexanone was used to explore the effects of solvent polarity and catalys

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