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211244-82-5

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211244-82-5 Usage

Type of compound

Heterocyclic aromatic organic compound

Structure

Contains a pyridine ring fused to a pyrimidine ring

Known for

Potential biological activity

Studied for

Potential pharmacological properties

Common use

Building block in the synthesis of pharmaceutical and medicinal compounds

Value in research

Unique structure and properties make it a valuable tool in medicinal and organic chemistry research

Check Digit Verification of cas no

The CAS Registry Mumber 211244-82-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,1,2,4 and 4 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 211244-82:
(8*2)+(7*1)+(6*1)+(5*2)+(4*4)+(3*4)+(2*8)+(1*2)=85
85 % 10 = 5
So 211244-82-5 is a valid CAS Registry Number.

211244-82-5Relevant articles and documents

GEM-DISUBSTITUTED HETEROCYCLIC COMPOUNDS AND THEIR USE AS IDH INHIBITORS

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Page/Page column 41-42, (2021/05/15)

The present invention relates to certain gem-disubstituted heterocyclic compounds, which modulate the activity of Isocitrate Dehydrogenase (IDH). The compounds of this invention are therefore useful in treating diseases caused by mutated IDH1 and/or mutat

Pyridopyrimidinone derivatives for treatment of neurodegenerative disease

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, (2008/06/13)

This invention provides pyridopyrimidines and 4-aminopyrimidines that are useful for treating cell proliferatives disorders, such as cancer and restenosis. We have now discovered a group of 7,8-dihydro-2 (amino and thio)pyrido[2,3-d]pyrimidines and 2,4-di

Pyrido[2,3-d]pyrimidin-7-one inhibitors of cyclin-dependent kinases

Barvian,Boschelli,Cossrow,Dobrusin,Fattaey,Fritsch,Fry,Harvey,Keller,Garrett,La,Leopold,McNamara,Quin,Trumpp-Kallmeyer,Toogood,Wu,Zhang

, p. 4606 - 4616 (2007/10/03)

The identification of 8-ethyl-2-phenylamino-8H-pyrido [2,3-d]pyrimidin-7-one (1) as an inhibitor of Cdk4 led to the initiation of a program to evaluate related pyrido [2,3-d]pyrimidin-7-ones for inhibition of cyclin-dependent kinases (Cdks). Analysis of m

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