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1H-Pyrazolo[3,4-d]pyrimidine, 1,4-diphenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

53645-78-6

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53645-78-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 53645-78-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,3,6,4 and 5 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 53645-78:
(7*5)+(6*3)+(5*6)+(4*4)+(3*5)+(2*7)+(1*8)=136
136 % 10 = 6
So 53645-78-6 is a valid CAS Registry Number.

53645-78-6Relevant academic research and scientific papers

BICYCLIC HETEROCYCLIC P-38 KINASE INHIBITORS

-

Page/Page column 56, (2008/06/13)

Provided are bicyclic heterocycle-based p38 kinase, including p38α and p38β kinase, inhibitors. Pharmaceutical compositions containing the compounds are also provided. Methods of use of the compounds and compositions are also provided, including methods of treatment, prevention, or amehoration of one or more symptoms of p38 kinase mediated diseases and disorders, including, but not limited to, inflammatory diseases and disorders.

Studies on Pyrazolopyrimidine Derivatives. XIII. Aryl Migration of 4-Aroyl-1H-pyrazolopyrimidines to 4-Aryl-4,5-dihydro-1H-pyrazolopyrimidine-4-carboxylic Acids

Higashino, Takeo,Matsushita, Yasuhiko,Takemoto, Masumi,Hayashi, Eisaku

, p. 3951 - 3958 (2007/10/02)

When a mixture of 4-aroyl-1-phenyl-1H-pyrazolopyrimidines (3) and sodium hydroxide in dimethyl sulfoxide (DMSO) was stirred for 1 h at room temperature, migration of the aryl group to the 4-position occurred, i.e., the benzilic acid rearrangement,

Aryl Coupling Reactions of Pyrazolopyrimidin-4-yl Radicals

Press, Jeffery B.,Eudy, Nancy H.,Morton, George O.

, p. 4605 - 4611 (2007/10/02)

4-Arylpyrazolopyrimidines (4) were the subjects of a synthetic investigation in order to evaluate their biological activity.Attempts to prepare 4 from 4-aminopyrazolopyrimidines (5) via classical Gomberg-Bachmann-Hey aryl coupling conditions failed.Conversion of 5 to 4 was accomplished by diazotiazation of 5 using alkyl nitrites with an acid catalyst in aromatic solvents.Isomer distribution of the aryl-coupled products 4 was that predicted for a radical intermediate (ortho > meta ca. para); isomer structures were assigned by a detailed 1H NMR analysis.Unusual fragmentation products 17 and 18 were isolated during the course of investigations.These oxadiazoles probably arise from collapse of intermediate pyrazolopyrimidin-4-yl radicals 15.

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