147057-13-4 Usage
Heterocyclic compound
Consists of a pyridine ring fused to an imidazole ring The compound is made up of two heterocyclic rings, which are rings containing more than one type of atom, in this case, carbon and nitrogen.
Imidazo[4,5-b]pyridine derivative
Classified as such due to the structure of the fused rings The compound is a derivative of the imidazo[4,5-b]pyridine structure, which is a core structure with various substituents.
Use in organic synthesis
Utilized in the creation of various chemical compounds The compound serves as a building block or intermediate in the synthesis of other organic compounds.
Pharmaceutical research
Employed in the development of drugs and pharmaceutical products Due to its unique structure and properties, 1H-Imidazo[4,5-b]pyridine,1,6-dimethyl-(9CI) is used in the creation and study of potential new medications.
Potential biological activities
Studied for its possible effects on biological systems Researchers are interested in understanding how 1H-Imidazo[4,5-b]pyridine,1,6-dimethyl-(9CI) interacts with living organisms, which could lead to the discovery of new therapeutic applications.
Pharmacological properties
Investigated for its potential effects on the body The compound's pharmacological properties are of interest for their potential use in treating various conditions and diseases.
Check Digit Verification of cas no
The CAS Registry Mumber 147057-13-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,7,0,5 and 7 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 147057-13:
(8*1)+(7*4)+(6*7)+(5*0)+(4*5)+(3*7)+(2*1)+(1*3)=124
124 % 10 = 4
So 147057-13-4 is a valid CAS Registry Number.
147057-13-4Relevant articles and documents
A convenient route to the imidazo[4,5-b]pyridines
Harada, Kenichi,Choshi, Tominari,Sugino, Eiichi,Sato, Koichi,Hibino, Satoshi
, p. 213 - 218 (2007/10/02)
The reaction of the acroleins possessing a leaving group, derived from alkenyl sulfides by Vilsmeier reaction, with 4-amino-1-methylimidazole provided a new and convenient route to the imidazo[4,5-b]pyridines, the reaction mechanisms of which were examined by a deuterium labelled experiment.
