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2-amino-4-(4-bromophenyl)-5,6-dihydro-6,7-dimethyl-5-oxo-4H-pyrano[3,2-c]pyridine-3-carbonitrile is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

882357-58-6

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882357-58-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 882357-58-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,8,2,3,5 and 7 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 882357-58:
(8*8)+(7*8)+(6*2)+(5*3)+(4*5)+(3*7)+(2*5)+(1*8)=206
206 % 10 = 6
So 882357-58-6 is a valid CAS Registry Number.

882357-58-6Downstream Products

882357-58-6Relevant academic research and scientific papers

Synthesis, characterization, and application of Cu2O and NiO nanoparticles supported on natural nanozeolite clinoptilolite as a heterogeneous catalyst for the synthesis of pyrano[3,2-b]pyrans and pyrano[3,2-c]pyridones

Baghbanian, Seyed Meysam

, p. 59397 - 59404 (2015/02/19)

In this research, Cu2O and NiO nanoparticles supported on natural nanozeolite clinoptilolite (CP) was found to be a recoverable catalyst system for synthesis of pyrano-[3,2-c]pyridone and pyrano[3,2-b]pyran derivatives in aqueous media. The nan

Practical and efficient synthesis of pyrano[3,2-c]pyridone, pyrano[4,3-b]pyran and their hybrids with nucleoside as potential antiviral and antileishmanial agents

Fan, Xuesen,Feng, Dong,Qu, Yingying,Zhang, Xinying,Wang, Jianji,Loiseau, Philippe M.,Andrei, Graciela,Snoeck, Robert,Clercq, Erik De

supporting information; experimental part, p. 809 - 813 (2010/05/18)

A highly practical and efficient preparation of pyrano[3,2-c]pyridone and pyrano[4,3-b]pyran derivatives was developed via an ionic liquid mediated and promoted multi-component reaction of aldehyde (1), 4-hydroxy-pyridin-2(1H)-one or 4-hydroxy-2-pyranone (2), and malononitrile (3). As an application, a series of pyrimidine nucleoside-pyrano[3,2-c]pyridone or pyrano[4,3-b]pyran hybrids were efficiently obtained. These hybrid compounds were evaluated as potential antiviral and antileishmanial agents and showed encouraging biological activities.

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