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4,4-dimethyl-2-ethyl-2-cyclohexen-1-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

69700-03-4

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69700-03-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 69700-03-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,9,7,0 and 0 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 69700-03:
(7*6)+(6*9)+(5*7)+(4*0)+(3*0)+(2*0)+(1*3)=134
134 % 10 = 4
So 69700-03-4 is a valid CAS Registry Number.

69700-03-4Downstream Products

69700-03-4Relevant academic research and scientific papers

DEHYDROGENATION REACTION

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Page/Page column 11-12, (2018/04/02)

The present invention relates to the field of organic synthesis and more specifically it concerns a process for the dehydrogenation of compound of formula (I) catalyzed by palladium (Pd0) in elemental metallic form.

Process for the preparation of cyclic ketones

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, (2008/06/13)

The invention provides a process for the preparation of cyclic ketones of the general formula STR1 in which R represents an optionally substituted alkyl or cycloalkyl group and R 1 and R 2 independently represent an optionally substituted alkyl, cycloalkyl or aryl group, which comprises heating a compound of the general formula STR2 in which X represents a chlorine or bromine atom and R is as defined above, with a compound of the general formula STR3 in which R 1 and R 2 are as defined above, in the presence of an organic acid.Certain cyclic ketones of formula (I) are useful as intermediates in the preparation of certain fungicidally active cyclopentane derivatives.

1,5-DICARBONYL COMPOUNDS A GENERAL PREPARATION METHOD

Duhamel, P.,Hennequin, L.,Poirier, J. M.,Tavel, G.,Vottero, C.

, p. 4777 - 4786 (2007/10/02)

In this report, a general method for the preparation of 1,5-dicarbonyl compounds and six membered ring annelation is described.This method involves the reaction of hemiacetal vinylogs 1 with enol ethers 2 or 3 in the presence of a Lewis acid.This reaction was successfully applied to the enol ethers of α and α,α'-hindered ketones such as 2,2,6-trimethyl cyclohexanone. α-Cyperone and 6-epi-α-cyperone were obtained using this process.

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