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3',5'-Dicyano-2',6'-dimethyl-1',4'-dihydro-2H-[3,4']bipyridinyl-1-carboxylic acid phenyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

106457-65-2

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106457-65-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 106457-65-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,6,4,5 and 7 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 106457-65:
(8*1)+(7*0)+(6*6)+(5*4)+(4*5)+(3*7)+(2*6)+(1*5)=122
122 % 10 = 2
So 106457-65-2 is a valid CAS Registry Number.

106457-65-2Downstream Products

106457-65-2Relevant academic research and scientific papers

Synthesis and Calcium Channel Antagonist Activity of Dialkyl 4-(Dihydropyridinyl)-1,4-dihydro-2,6-dimethyl-3,5-pyridinecarboxylates

Dagnino, Lina,Li-Kwong-Ken, Moy Cheong,Wynn, Hla,Wolowyk, Michael W.,Triggle, Christopher R.,Knaus, Edward E.

, p. 640 - 646 (2007/10/02)

The sodium borohydride reduction of 3,5-disubstituted 1,4-dihydro-2,6-dimethyl-4-(pyridinyl)pyridines 2 and 5 in the presence of methyl, phenyl, or tert-butyl chloroformate afforded the respective 4-(dihydropyridinyl)-1,4-dihydropyridines 4 and 6 in good yield.Products 4 comprised a mixture of the 1,2- and 1,6-dihydropyridinyl regioisomers 4a and 4b where 4a was always the predominant regioisomer.Compounds possessing a 4- substituent, such as 26, were also a mixture of two regioisomers 26a and 26b, and each regioisomer existed as a mixture of two rotamers in Me2SO-d6 at 25 deg C (26a',26a", and 26b',26b") due to restricted rotation about the nitrogen-to-carbonyl carbamate bond.The calcium antagonist activities for 4 and 6 were determined by using the muscarinic receptor-mediated Ca2+-dependent contraction of guinea pig ileal longitudinal smooth muscle.The relative order of activities for the 4-(dihydropyridinyl) analogues was 4-(dihydro-3-pyridinyl) > 4-(dihydro-4-pyridinyl).Increasing the size of the C-3(5) alkyl ester substituents increased activity.Compounds having nonidentical ester substituents were more active than those having identical ester substituents.Replacement of the C-3 and/or C-5 ester substituents by a cyano substituent(s) decreased activity significantly.An approximate 1:1 correlation between the IC50 value for inhibition of nitrendipine binding and inhibition of the tonic component of the muscarinic-induced contractile response was observed.The test results suggest that a 4-(dihydropyridinyl) substituent is bioisosteric with a 4-(nitrophenyl) substituent on a 1,4-dihydropyridine ring where m- and p-nitrophenyl are bioisosteric with the 4- 4 and 4-(1,2-dihydro-4-pyridinyl) 6 isomers, respectively.

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