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Pyrido[2,3-d]pyrimidine-6-carbonitrile, 7-amino-1,2,3,4-tetrahydro-3-methyl-2,4-dioxo-5-phenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

95548-68-8

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95548-68-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 95548-68-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,5,5,4 and 8 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 95548-68:
(7*9)+(6*5)+(5*5)+(4*4)+(3*8)+(2*6)+(1*8)=178
178 % 10 = 8
So 95548-68-8 is a valid CAS Registry Number.

95548-68-8Downstream Products

95548-68-8Relevant academic research and scientific papers

Arylidenemalononitriles in Heterocyclic Syntheses: a Novel Synthesis of Pyridopyrimidines

Gogoi, Mukti,Bhuyan, Pulakjyoti,Sandhu, Jagir S.,Baruah, Jogendra N.

, p. 1549 - 1550 (1984)

Arylidenemalononitriles react with 6-amino and 6-hydroxyamino-1,3-dimethyl- and 3-methyl-pyrimidine-2,4(1H,3H)-dione to give pyridopyrimidines in good yields.

New strategy for the oxidation of Hantzsch 1,4-dihydropyridines and dihydropyrido[2,3-d]pyrimidines catalyzed by DMSO under aerobic conditions

Saini, Anil,Kumar, Sanjay,Sandhu, Jagir S.

, p. 2317 - 2324 (2008/02/09)

A novel metal-salt-oxidant-free, efficient, and economical method for the oxidation of Hantzsch 1,4-dihydropyridines that uses aerial oxygen and solvent-grade dimethylsulfoxide is described. Also, the synthesis of pyrido[2,3-d]pyrimidines is achieved from in situ oxidation of dihydropyrido[2,3-d]pyrimidines that arise from the reaction of 6-aminouracils and cyano olefins in dimethylsulfoxide. Copyright Taylor & Francis Group, LLC.

A novel three-component one-pot synthesis of pyrano[2,3-d]pyrimidines and pyrido[2,3-d]pyrimidines using microwave heating in the solid state

Devi, Ipsita,Kumar,Bhuyan, Pulak J.

, p. 8307 - 8310 (2007/10/03)

Microwave-assisted three-component cyclocondensation of barbituric acids 1, benzaldehyde 2 and alkyl nitriles 3 proceeds in the absence or presence of triethylamine to afford pyrano[2,3-d]pyrimidines 4 and 6-aminouracils 5 or 6-hydroxyaminouracils 6 react with 2 and 3 under identical conditions to yield pyrido[2,3-d]pyrimidines 7, all in high yields.

Studies on Uracils. 10. A Facile One-Pot Synthesis of Pyrido- and Pyrazolopyrimidines

Bhuyan, Pulakjyoti,Boruah, Romesh Chandra,Sandhu, Jagir Singh

, p. 568 - 571 (2007/10/02)

The reaction of functionalised uracils bearing amino and hydroxyamino groups at C-6 position (4 and 5) with strongly electrophilic cyano olefins (1,2 and 3) gave rise to pyridopyrimidines 7-9 in excellent yields.Hydrazine-substituted uracil 6 gave access to an efficient one-step synthesis of pyrazolopyrimidines 10.The capture of an eliminated hydrogen molecule by cyano olefins in the case of their reaction with 4 and 6 was confirmed by the isolation of dihydrocyano olefins.This fact further supported the plausible mechanism for the formation of compounds 7-10 via dihydropyrido- and dihydropyrazolopyrimidine intermediates A and C.

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