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4-(2-FURYL)-2-OXO-1,2-DIHYDRO-3-PYRIDINECARBONITRILE is a complex organic chemical compound with the molecular formula C10H6N2O2. It is characterized by a pyridine ring, which is a six-membered aromatic ring containing two nitrogen atoms, and a furyl group, which is a five-membered aromatic ring with one oxygen atom. The compound features a carbonitrile group (-CN) attached to the pyridine ring, and a keto group (C=O) adjacent to the furyl group. This molecule is a derivative of 3-pyridinecarbonitrile and is known for its potential applications in the synthesis of various pharmaceuticals and agrochemicals due to its unique structure and reactivity. It is important to note that handling and use of this chemical should be done with caution, as it may have specific safety and health considerations.

174713-66-7

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174713-66-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 174713-66-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,4,7,1 and 3 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 174713-66:
(8*1)+(7*7)+(6*4)+(5*7)+(4*1)+(3*3)+(2*6)+(1*6)=147
147 % 10 = 7
So 174713-66-7 is a valid CAS Registry Number.

174713-66-7Downstream Products

174713-66-7Relevant academic research and scientific papers

Enaminones as building blocks in heterocyclic syntheses: Reinvestigating the product structures of enaminones with malononitrile. A novel route to 6-substituted-3-oxo-2,3-dihydropyridazine-4-carboxylic acids

Alnajjar, Abdul-Aziz,Abdelkhalik, Mervat Mohammed,Al-Enezi, Amal,Elnagdi, Mohamed Hilmy

body text, p. 68 - 77 (2009/08/15)

The reported structures of reaction products of enaminones with malononitrile in ethanolic piperidine are revised. A novel route to 2,3-dihydropyridazine-4-carboxylic acids 4a-c via reactions of 2-cyano-5-(dimethylamino)-5-arylpenta-2,4-dienamides 8a-c wi

1-Substituted 3-Dimethylaminoprop-2-en-1-ones as Building Blocks in Heterocyclic Synthesis: Routes to 6-Aryl and 6-Heteroaryl-2H-pyran-2-ones and 6- and 4-Aryl-pyridin-2(1H)-ones

Al-Omran, Fatima,Al-Awadhi, Nouria,Khalik, Mervat Mohammed Abdel,Kaul, Kamini,EL-Khair, Adel Abu,Elnagdi, Mohammed Hilmy

, p. 601 - 615 (2007/10/03)

Several new 6-substituted-3-acylamino-2H-pyran-2-ones 6 a-j are prepared from the reaction of the enaminones 4 a-f with N-acyl- and N-benzoyl-glycines. The enaminones 4 a-c react with malononitrile in ethanol solution and in presence of a base to yield th

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