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3-Pyridinecarbonitrile, 4-(4-chlorophenyl)-1,2-dihydro-5,6-dimethyl-2-oxo- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

65429-80-3

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65429-80-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 65429-80-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,5,4,2 and 9 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 65429-80:
(7*6)+(6*5)+(5*4)+(4*2)+(3*9)+(2*8)+(1*0)=143
143 % 10 = 3
So 65429-80-3 is a valid CAS Registry Number.

65429-80-3Downstream Products

65429-80-3Relevant academic research and scientific papers

Efficient one-pot four-component synthesis and X-ray crystallographic structure of 2-pyridone derivatives

Balalaie, Saeed,Hashemi, Mohammed M.,Khezri, S. Hadi,Rominger, Frank,Ghabraie, Elmira,Oeser, Thomas

, p. 1272 - 1280 (2013)

A series of 3-cyano-2-pyridone derivatives were synthesized by one-pot four-component condensation reaction involving a benzaldehyde derivative, alkyl cyanoacetate, acyclic or cyclic ketones, and ammonium acetate in reflux condition. The X-ray structure of the products 5a and 5d confirm symmetric dimers via hydrogen bonding interactions between individual pyridine molecules showing, in addition, also π-π stacking interactions.

Enzymatic multicomponent reaction for simultaneous synthesis of two important scaffolds, pyridin-2-ones and α-alkylated nitriles

Liu, Zhi-Qiang,Hu, Yu-Jing,Chen, Xiao-Yang,Wu, Qi,Lin, Xian-Fu

, p. 663 - 668 (2015)

An efficient approach for the synthesis of highly substituted pyridin-2-one derivatives and α-alkylated nitriles through enzymatic multicomponent reaction (MCR) was developed. This MCR involved bio-mimetic reduction between 3,4-dihydropyridin-2-one and activated olefin, both of which were in situ generated in the Acylase Amano (AA)-catalyzed domino reaction starting from benzaldehyde, cyanoacetamide and ketone. A wide range of substituted benzaldehydes and ketones were accepted by this reaction. Both final products (pyridin-2-one derivatives and α-alkylated nitriles) were important skeletons and synthetic intermediates. The synthetic application of prepared α-alkylated nitrile was demonstrated by converting it into the corresponding α-alkyl-β2-amino acid with high yield.

Cascade synthesis of 2-pyridones using acrylamides and ketones

Rai, Sunil K.,Khanam, Shaziya,Khanna, Ranjana S.,Tewari, Ashish K.

, p. 44141 - 44145 (2015/02/02)

Microwave assisted non-catalytic condensation of 2-cyanoacetamide with aromatic aldehydes, and enolate mediated Michael-type addition to acrylamide followed by oxidative cyclization, produce 2-pyridones in good to excellent yield. Unsymmetrical ketones produce two regioisomeric enolates, therefore thermodynamic and kinetic products of butan-2-one and pentan-2-one have been isolated and fully characterized. This journal is

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