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2-amino-4-(3-nitrophenyl)-5-oxo-5H-chromeno[4,3-b]pyridine-3-carbonitrile is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1428871-89-9

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1428871-89-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1428871-89-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,2,8,8,7 and 1 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1428871-89:
(9*1)+(8*4)+(7*2)+(6*8)+(5*8)+(4*7)+(3*1)+(2*8)+(1*9)=199
199 % 10 = 9
So 1428871-89-9 is a valid CAS Registry Number.

1428871-89-9Downstream Products

1428871-89-9Relevant academic research and scientific papers

Immobilized TiO2 nanoparticles on carbon nanotubes: An efficient heterogeneous catalyst for the synthesis of chromeno[: B] pyridine derivatives under ultrasonic irradiation

Abdolmohammadi, Shahrzad,Mirza, Behrooz,Vessally, Esmail

, p. 41868 - 41876 (2019/12/28)

A new protocol for the synthesis of chromeno[b]pyridine derivatives is described via a three-component reaction of 4-aminocoumarin, aromatic aldehydes and malononitrile catalyzed by TiO2 nanoparticles immobilized on carbon nanotubes (TiO2

Solvent-free synthesis of novel 5-oxo-5H-chromeno[4,3-b]pyridine derivatives

Motamedi

, p. 1839 - 1843 (2013/07/26)

An efficient and simple method for the synthesis of new 5-oxo-5H-chromeno[4,3-b]pyridine derivatives via Michael addition of 4-aminocoumarin to arylidenemalononitrile for 20 min at 150 C without any solvent is proposed. The advantages of this procedure ar

Facile synthesis of pyridopyrimidine and coumarin fused pyridine libraries over a Lewis base-surfactant-combined catalyst TEOA in aqueous medium

Bhattacharyya, Pranabes,Paul, Sanjay,Das, Asish R.

, p. 3203 - 3208 (2013/03/28)

A highly convergent and efficient protocol, for the facile synthesis of a library of coumarin fused pyridine and pyridopyrimidine derivatives, has been developed by applying a Lewis base-surfactant-combined catalyst (LBSC) triethanolamine (TEOA). The method described has the benefits of operational simplicity and excellent yields of the targeted molecule. The LBSCs were found to form stable colloidal dispersions rapidly in the presence of reaction substrates in water, even when the substrates are solid. In light of the increased demand for reduction of organic solvents in industry, the surfactant aided Lewis base catalysis described here may have immense practical consequences in organic synthesis. This work may not only lead to environmentally benign systems but also will provide a newer aspect of organic chemistry in water.

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