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1-<1-Ethyl-hexa-1,2-dienyl>-cyclohexanol is a complex organic compound with the molecular formula C14H24O. It features a cyclohexanol group (a cyclohexane ring with a hydroxyl group) and a 1-ethyl-hexa-1,2-dienyl moiety (a hexadiene chain with an ethyl group attached to the first carbon). This chemical is characterized by its unique structure, which includes a six-carbon ring with a double bond in the 1,2-position and an ethyl group attached to the first carbon of the diene. The compound may have potential applications in the synthesis of various organic compounds and materials, but further research is needed to explore its properties and uses.

1518-34-9

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1518-34-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1518-34-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,5,1 and 8 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1518-34:
(6*1)+(5*5)+(4*1)+(3*8)+(2*3)+(1*4)=69
69 % 10 = 9
So 1518-34-9 is a valid CAS Registry Number.

1518-34-9Relevant academic research and scientific papers

SYNTHESE D'ALCOHOLS α-ALLENIQUES PAR REACTION D'ORGANOCHROMIQUES PROPARGYLIQUES SUR LES ALDEHYDES ET LES CETONES

Place, Pierre,Verniere, Catherine,Gore, Jacques

, p. 1359 - 1368 (2007/10/02)

Propargylic bromides can be condensed with aldehydes and ketones in the presence of Hiyama's reagent (2CrCl3+LiAlH4 in THF) leading to α-allenic alcohols, to homopropargylic alcohols or to the mixture of both of them.The selectivity (or specificity) of this reaction depends on the substitution of the propargylic bromide, on the structure of the ketone, and on the presence of HMPT in the reaction mixture.In many cases, α- allenic alcohol has been specifically or very selectively obtained.The mechanism of the reaction and the influence of the various parameters are discussed.

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