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Cyclohexanone, 2,6-bis(phenylmethyl)-, (2R,6R)-rel- is a chiral organic compound with the molecular formula C20H22O. It is a derivative of cyclohexanone, featuring two phenylmethyl groups attached to the 2nd and 6th carbon atoms of the cyclohexane ring. The compound exhibits a specific stereochemistry, with the R configuration at both the 2nd and 6th positions, indicating that the hydroxyl group is on the right side when looking at the molecule from the perspective of the carbon atom with the lowest编号. Cyclohexanone, 2,6-bis(phenylmethyl)-, (2R,6R)-rel- is of interest in organic chemistry and pharmaceutical research due to its unique structure and potential applications in the synthesis of various compounds.

7382-10-7

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7382-10-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7382-10-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,3,8 and 2 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 7382-10:
(6*7)+(5*3)+(4*8)+(3*2)+(2*1)+(1*0)=97
97 % 10 = 7
So 7382-10-7 is a valid CAS Registry Number.

7382-10-7Relevant academic research and scientific papers

α-Benzylation of Ketones by Reaction with Benzylamine. Regioselective Reduction of C-C Double Bonds in Cohjugated Enones

Armesto, Diego,Esteban, Soledad,Horspool, William M.,Martin, Juan-Antonio F.,Martinez-Alcazar, Paz,Perez-Ossorio, Rafael

, p. 751 - 755 (2007/10/02)

Prolonged reaction of some ketones with benzylamine at reflux converts them into α-benzyl derivatives by a route involving Aldol condensation of the related ketimine with benzaldimine followed by exclusive reduction of the resultant C-C double bond.Reduction does not occur when pure benzylamine is used under oxygen-free nitrogen, however the inclusion of a trace of benzaldehyde restores the efficiency of the reaction.Treatment of several ketones in this manner established the scope of the process.When the reaction was extended to the reduction of α,β-unsaturated enones again using benzylamine, reaction times were shorter and the product yield greater.The possibility that the reductive step was an intramolecular 1,5-hydrogen transfer was studied.

SELECTIVE REDUCTION OF C-C DOUBLE BONDS IN CONJUGATED ENONES BY BENZYLAMINE. A VARIANT OF THE SOMMELET REACTION

Armesto, Diego,Horspool, William M.,Martin, Juan Antonio F.,Perez-Ossorio, Rafael

, p. 5217 - 5220 (2007/10/02)

Prolonged reaction of some ketones with benzylamine at reflux converts them into α-benzyl derivatives by a route involving aldol condensation of the related ketimine with benzaldimine followed by exclusive reduction of the resultant C-C double bond by hydride transfer from benzylamine.This efficient procedure is a variant of the Sommelet reaction for the synthesis of aldehydes.

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