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(R)-2-[1-Hydroxy-meth-(Z)-ylidene]-3-methyl-cyclohexanone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

97590-64-2

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97590-64-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 97590-64-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,7,5,9 and 0 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 97590-64:
(7*9)+(6*7)+(5*5)+(4*9)+(3*0)+(2*6)+(1*4)=182
182 % 10 = 2
So 97590-64-2 is a valid CAS Registry Number.

97590-64-2Relevant academic research and scientific papers

First stereoselective synthesis of (4aS,5R)-4,4a,5,6,7,8-hexahydro-4a,5- dimethyl-2(3H)-naphthalenone

Cuesta, Xavier,Gonzalez, Asensio,Bonjoch, Josep

, p. 3365 - 3370 (1999)

The synthesis of enantiomerically pure (4aS,5R)-hexahydro-4a,5-dimethyl- 2(3H)-naphthalenone (-)-1 is described for the first time. The synthesis starts from (R)-3-methylcyclohexanone and involves the preparation of Piers enol lactone 6 in its enantiopure

REGIOSELECTIVE SYNTHESIS OF OPTICALLY ACTIVE (R)-5-METHYL- AND (R)-7-METHYL-5,6,7,8-TETRAHYDROQUINOLINES

Chelucci, Giorgio,Cossu, Sergio,Scano, Gianfranco,Soccolini, Francesco

, p. 1397 - 1403 (2007/10/02)

Five synthesis routes have been evaluated for the regioselective preparation of (R)-5-methyl- and (R)-7-methyl-5,6,7,8-tetrahydroquinolines from (+)-(R)-3-methylcyclohexanone.

Optical Rotatory Dispersion Studies. 138. Synthesis and Conformational Analysis of β-Heteroatom-Substituted Cyclohexanones

Gorthey, Lee Ann,Vairamani, Mariappandar,Djerassi, Carl

, p. 4173 - 4182 (2007/10/02)

Circular dichroism and proton magnetic resonance spectroscopy were used in the conformational analysis of a series of β-heteroatom-substituted cyclohexanones.It was found that the axial population of the substituted ketone relative to that of the monosubstituted cyclohexanone is enhanced for the more highly electronegative substituents oxygen and fluorine and decreased for the less electronegative substituents chlorine, bromine, and sulfur.Possible mechanisms underlying this behavior, including electrostatic and dipole-dipole interactions as well as through-space and through-bond orbital interactions, are briefly discussed.

Conformational Studies of R-(+)-2-Alkylidene- and R-(-)-2-Benzylidene-5-methylcyclohexanones

Anand, Devinder K.,Hargreaves, Michael K.,Khan, Mohsin A.

, p. 978 - 988 (2007/10/02)

The cis and trans 2-alkylidene-5-methylcyclohexanones have been separated and distinguished. 2-Benzylidene-5-methylcyclohexanone was also prepared in both forms.The CD, ORD, UV and IR spectra are recorded and discussed.The NMR data include solvent and tem

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