1000518-77-3 Usage
Derivative of pyridine
The compound is derived from pyridine, a heterocyclic aromatic compound.
Methyl group attachment
A methyl group is attached to the third carbon atom of the pyridine ring.
Pharmaceutical research and drug development
The compound has potential therapeutic properties and is used in pharmaceutical research and drug development.
Anti-inflammatory effects
2-(5-methylpyridin-3-yl)acetic acid has been studied for its potential anti-inflammatory effects.
Anti-cancer effects
The compound has also been studied for its potential anti-cancer effects.
Organic synthesis
The compound may have applications in the field of organic synthesis.
Building block for complex molecules
2-(5-methylpyridin-3-yl)acetic acid can be used as a building block for the creation of other complex molecules.
Check Digit Verification of cas no
The CAS Registry Mumber 1000518-77-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,0,0,5,1 and 8 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1000518-77:
(9*1)+(8*0)+(7*0)+(6*0)+(5*5)+(4*1)+(3*8)+(2*7)+(1*7)=83
83 % 10 = 3
So 1000518-77-3 is a valid CAS Registry Number.
1000518-77-3Relevant articles and documents
DIBENZOTHIOPHENE DERIVATIVES AS DNA- PK INHIBITORS
-
Page/Page column 67, (2010/12/26)
Compound formula I: wherein: X1 and X2 may be either (a) C and O, (b) N and N, or (c) C and NH, where the dotted bonds represents a double bond in the appropriate location; R1 and R2 are independently selected from hydrogen, an optionally substituted C1-7 alkyl group, an optionally substituted C3-20 heterocyclyl group, or an optionally substituted C5-20 aryl group, or may together form, along with the nitrogen atom to which they are attached, an optionally substituted heterocyclic ring having from 4 to 8 ring atoms; RN1 is selected from hydrogen and an optionally substituted C1-4 alkyl group; RC1 is selected from an optionally substituted C1-7 alkyl group, an optionally substituted C3-20 heterocyclyl group, or an optionally substituted C5-20 aryl group; or RN1 and RC1 may together form an optionally substituted C2-4 alkylene group.
