1190212-21-5 Usage
Molecular weight
222.26 g/mol The molecular weight is the mass of one mole of the compound, calculated by adding the atomic weights of all the atoms in the molecular formula.
Structure
1H-Pyrrolo[2,3-b]pyridine-2-carboxylic acid, 4,6-dimethyl-, methyl ester The structure consists of a pyrrolo[2,3-b]pyridine core with a carboxylic acid group, dimethyl substituents at positions 4 and 6, and a methyl ester group.
Heterocyclic compound
Yes The compound contains a ring structure with both carbon and nitrogen atoms, making it a heterocyclic compound.
Methyl ester derivative
Yes The compound has a methyl ester group, making it a derivative of the parent compound 1H-Pyrrolo[2,3-b]pyridine-2-carboxylic acid, 4,6-dimethyl.
Pharmaceutical applications
Potential The compound has potential pharmaceutical applications due to its unique structure and properties.
Organic synthesis and drug discovery
Commonly used The methyl ester form of the compound is often used in organic synthesis and drug discovery processes because of its unique chemical properties.
Building block in synthesis
Yes The compound serves as a building block in the synthesis of various pharmaceuticals and biologically active compounds.
Research and development tool
Valuable The specific structure of the compound makes it a valuable tool for research and development in the field of medicinal chemistry.
Check Digit Verification of cas no
The CAS Registry Mumber 1190212-21-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,9,0,2,1 and 2 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1190212-21:
(9*1)+(8*1)+(7*9)+(6*0)+(5*2)+(4*1)+(3*2)+(2*2)+(1*1)=105
105 % 10 = 5
So 1190212-21-5 is a valid CAS Registry Number.
1190212-21-5Relevant articles and documents
Synthesis of Substituted Imidazo[1, 5-a]pyrimidines, 1H-pyrrolo[2, 3-b]pyridines and 3-methyl-3H-imidazo[4, 5-b]pyridines
Wu, Jingshing,Xing, Xuechao,Cuny, Gregory D.
experimental part, p. 203 - 207 (2010/04/23)
Cyclization of in situ generated 5-aminoimidazoles with various malondialdehydes or 1, 3-diketones gave substituted imidazo[1, 5-a]pyrimidines. However, cyclization of 2-aminopyrroles and 5-amino-1-methylimidazoles resulted in condensations on a carbon at
