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Cyclohexane, 1-ethyl-3-methyl, trans- is an organic compound with the molecular formula C9H18. It is a cyclic alkane with a six-carbon ring structure, where one carbon atom is substituted with an ethyl group (C2H5) and another carbon atom is substituted with a methyl group (CH3). The "trans" descriptor indicates that the ethyl and methyl groups are positioned on opposite sides of the ring, with the maximum possible spatial separation. Cyclohexane, 1-ethyl-3-methyl-, trans- is a member of the cycloalkane family and is known for its relatively stable and non-reactive nature due to the absence of double bonds or other reactive functional groups. It is used in various chemical applications, including as a solvent or a precursor in the synthesis of more complex organic molecules.

4926-76-5

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4926-76-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4926-76-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,9,2 and 6 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 4926-76:
(6*4)+(5*9)+(4*2)+(3*6)+(2*7)+(1*6)=115
115 % 10 = 5
So 4926-76-5 is a valid CAS Registry Number.

4926-76-5Downstream Products

4926-76-5Relevant academic research and scientific papers

Organolanthanide catalyzed hydrogenation and hydrosilylation of substituted methylenecycloalkanes

Molander, Gary A.,Winterfeld, Joern

, p. 275 - 279 (1996)

This communication presents a study of the scope of the catalytic hydrogenation and hydrosilylation of chiral exomethylene-substituted cyclopentanes and cyclohexanes utilizing the organolanthanide precatalysts Cp2* LnCH(SiMe3)2 (Cp* = C5Me5; Ln = Sm, Yb). Both reaction types are sterically driven and lead to the cis-diastereomer as the major product. Additionally, the hydrosilylation is regiospecific, the silane being placed exclusively at the terminal position of the double bond.

CATALYTIC ACTIVITY OF Pt/AlPO4 AND RELATED SYSTEMS. II. GAS PHASE HYDROGENATION OF XYLENES

Aramendia, M. A.,Borau, V.,Jimenez, C.,Marinas, J. M.

, p. 743 - 750 (2007/10/02)

In the present paper data are reported on the gas-phase hydrogenation of o-, m-, and p-xylene and o-, m-, p-ethylmethylbenzene using a pulse reactor.New systems obtained by supporting Pt on AlPO4-Al2O3 (75/25), pure AlPO4 and SiO4-AlPO4 (80/20) have been used as catalysts.The effect of the reduction temperature of the catalysts and the hydrogen pressure on the selectivity to cis- and trans-dimethylcyclohexanes and ethylmethylcyclohexanes has been investigated.The result obtained are interpreted by assuming a Horiuti-Polanyi mechanism, with suprafacial addition of hydrogen.

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