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Cyclohexanecarboxylic acid, 1-(2-oxopropyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

72349-79-2

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72349-79-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 72349-79-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,2,3,4 and 9 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 72349-79:
(7*7)+(6*2)+(5*3)+(4*4)+(3*9)+(2*7)+(1*9)=142
142 % 10 = 2
So 72349-79-2 is a valid CAS Registry Number.

72349-79-2Relevant academic research and scientific papers

Michael Reaction of Conjugated Nitro Olefins with Carboxylic Acid Dianions and with Ester Enolates: New Synthesis of γ-Keto Acids and γ-Keto Esters

Miyashita, Masaaki,Yamaguchi, Ryuji,Yoshikoshi, Akira

, p. 2857 - 2863 (2007/10/02)

Base-sensitive conjugated nitro olefins 2 reacted with lithium dianions of carboxylic acids 3 or with lithium enolates of esters 4 at a low temperature of ca. -100 deg C, and subsequent treatment of the Michael adducts with aqueous acid yielded γ-keto acids 5 or esters 5' in a one-pot operation, respectively.Results of both the reactions have been compared.Some applications of the resulting γ-keto esters in organic synthesis have also been demonstrated in lactone synthesis and cyclenone annulation.

NEW SYNTHESIS OF Γ-KETO ACIDS FROM NITROOLEFINS AND CARBOXYLIC ACID DIANIONS

Miyashita, Masaaki,Yamaguchi, Ryuji,Yoshikoshi, Akira

, p. 1505 - 1508 (2007/10/02)

As a convenient synthetic method of γ-keto acids, oxoalkylation of carboxylic acids with nitroolefins was examinated.Carboxylic acid dianions reacted with conjugated nitroolefins at low temperature (-100 deg C) and a variety of γ-keto acids were obtained on acidic workup in moderate to good yields.

Pharmaceutically active cyclohexyl compounds and their preparation

-

, (2008/06/13)

The chemical compounds of the invention are useful as the active compound in drugs because of their anticonvulsant and/or antianoxic activity. They have the general formula STR1 wherein Z is a hydroxyl group; a group--OM wherein M is an alkali metal atom or an equivalent atom fraction of an alkaline-earth metal or an amino group such as --NH2, and R is a linear or branched alkyl group containing from 1 to 9 carbon atoms, and optionally substituted by one or more halogen atoms; a linear or branched alkenyl or alkynyl, alkoxyalkyl, or acylalkyl group containing from 2 to 9 carbon atoms and optionally substituted by one or more halogen atoms; an aryl or arylalkyl or aryloxyalkyl group comprising at least one aromatic radical and an alkyl chain having from 1 to 4 carbon atoms.

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