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2-(4-(N-methyl-N-phenylamino)-5H-chromeno[2,3-d]pyrimidin-2-yl)phenol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1430822-99-3

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1430822-99-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1430822-99-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,3,0,8,2 and 2 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1430822-99:
(9*1)+(8*4)+(7*3)+(6*0)+(5*8)+(4*2)+(3*2)+(2*9)+(1*9)=143
143 % 10 = 3
So 1430822-99-3 is a valid CAS Registry Number.

1430822-99-3Downstream Products

1430822-99-3Relevant academic research and scientific papers

Synthesis, Characterization, and Heterogeneous Catalytic Activity of Sulfamic Acid Functionalized Magnetic IRMOF-3

Mostafavi, Mohammad Mahdi,Movahedi, Farnaz

, p. 787 - 793 (2019/02/09)

In this work, post-synthesis modification of Fe3O4/IRMOF-3 nanocomposite with chlorosulfonic acid groups afforded sulfamic acid-functionalized magnetic metal-organic frameworks (Fe3O4/IRMOF-3/SO3H). F

Novel approaches for the synthesis of a library of fluorescent chromenopyrimidine derivatives

Zonouzi, Afsaneh,Hosseinzadeh, Fatemeh,Karimi, Nastaran,Mirzazadeh, Roghieh,Ng, Seik Weng

, p. 240 - 246 (2013/06/26)

A library of some new fluorescent chromenopyrimidine derivatives has been synthesized by new approaches. Water-promoted and one-pot reaction can produce new dialkylylamino)-5H-chromeno[2,3-d]pyrimidin-2-yl) phenols. These compounds can also be produced using domino reaction. Two parallel methods are compared. Novel N-alkyl-N-phenyl-5H-chromeno[2,3-d]-pyrimidin-4-amines and 4-alkoxy-5H-chromeno[2, 3-d]pyrimidines are synthesized by Lewis-acid catalyzed reactions. The fluorescence emission intensity of the four compounds from each of libraries after excitation in 290 nm is measured. Compound 2-(4,5-bis(N-methyl-N-phenylamino)-5H-chromeno[2,3-d]pyrimidin-2-yl)phenol was isolated as a byproduct. The details of an interesting exchangeable intramolecular H- bonding of two of the new compounds are reported by X-ray analysis data.

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