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methyl (S)-4-(dimethyl(phenyl)silyl)-6-(2-[1,3]dioxolan-2-ylethyl)-1-[(1S,5R)-5,8,8-trimethyl-2-oxo-3-oxabicyclo[3.2.1]oct-1-ylcarbonyl]-1,6-dihydropyridine-3-carboxylate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

497075-36-2

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497075-36-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 497075-36-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,9,7,0,7 and 5 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 497075-36:
(8*4)+(7*9)+(6*7)+(5*0)+(4*7)+(3*5)+(2*3)+(1*6)=192
192 % 10 = 2
So 497075-36-2 is a valid CAS Registry Number.

497075-36-2Relevant academic research and scientific papers

First asymmetric syntheses of 6-substituted nipecotic acid derivatives

Hoesl, Cornelia E.,H?fner,Wanner, Klaus T.

, p. 307 - 318 (2007/10/03)

Various nipecotic acid derivatives are known to be potent GABA uptake inhibitors thus being useful in the treatment of a number of neurological and psychological disorders. In this paper, the first asymmetric syntheses of 6-substituted nipecotic acid deri

Generation of chiral N-acylpyridinium ions by means of silyl triflates and their diastereoselective trapping reactions: Formation of N-acyldihydropyridines and N-acyldihydropyridones

Hoesl, Cornelia E,Maurus, Markus,Pabel, J?rg,Polborn, Kurt,Wanner, Klaus Th

, p. 6757 - 6770 (2007/10/03)

An efficient method for the generation of chiral N-acylpyridinium salts from various pyridines and a chiral acid chloride promoted by means of silyl triflates as additives is presented. The stereoselective addition of organometallic reagents to the intermediate chiral N-acylpyridinium ions led to α-substituted N-acyldihydropyridines and N-acyldihydropyridones in good yields, whereas no or minor amounts of products were obtained, when standard procedures without silyltriflates as additives were employed. Good diastereoselectivities were observed dependent on which pyridine or organometallic reagents were used. The removal of the chiral auxiliary proceeded smoothly either under basic or reductive reaction conditions.

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