219762-28-4 Usage
Uses
Used in Pharmaceutical Industry:
5-bromo-2-methyl-3H-imidazo[4,5-b]pyridine is utilized as a key intermediate in the synthesis of various pharmaceuticals due to its unique chemical structure. It contributes to the development of new drugs with potential therapeutic applications.
Used in Agrochemical Industry:
In the agrochemical sector, 5-bromo-2-methyl-3H-imidazo[4,5-b]pyridine serves as a building block for the creation of novel agrochemicals, potentially enhancing crop protection and yield.
Used in Antitumor Applications:
5-bromo-2-methyl-3H-imidazo[4,5-b]pyridine is employed as an antitumor agent, showing promise in the development of treatments for various types of cancer. Its specific mechanism of action and efficacy in combating tumor growth are under investigation.
Used in Neurological Disorder Treatment:
5-bromo-2-methyl-3H-imidazo[4,5-b]pyridine has been studied for its potential use in treating neurological disorders, suggesting that it may have neuroprotective or other beneficial effects on the nervous system.
Used in Antimicrobial Applications:
5-bromo-2-methyl-3H-imidazo[4,5-b]pyridine has demonstrated antimicrobial properties, indicating its potential use in the development of new antibiotics or antifungal agents to combat resistant strains.
Used in Antiviral Applications:
5-bromo-2-methyl-3H-imidazo[4,5-b]pyridine has also been investigated for its antiviral properties, suggesting a possible role in the development of treatments for viral infections.
While the full spectrum of applications for 5-bromo-2-methyl-3H-imidazo[4,5-b]pyridine is still being explored, its versatility and potential across multiple fields of research highlight its value as a significant chemical compound. Further research is necessary to fully understand and harness its capabilities in various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 219762-28-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,9,7,6 and 2 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 219762-28:
(8*2)+(7*1)+(6*9)+(5*7)+(4*6)+(3*2)+(2*2)+(1*8)=154
154 % 10 = 4
So 219762-28-4 is a valid CAS Registry Number.
InChI:InChI=1/C7H6BrN3/c1-4-9-5-2-3-6(8)11-7(5)10-4/h2-3H,1H3,(H,9,10,11)
219762-28-4Relevant academic research and scientific papers
INHIBITORS OF FIBROBLAST GROWTH FACTOR RECEPTOR KINASES
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Paragraph 00430-00432, (2021/12/28)
Provided herein are heteroaryl inhibitors of fibroblast growth factor receptor kinases, pharmaceutical compositions comprising said compounds, and methods for using said compounds for the treatment of diseases.
Sulfonamide compounds and uses thereof as medicines
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, (2008/06/13)
The present invention relates to a sulfonamide compound of the formula (I): wherein each symbol is as defined in the specification, a salt thereof, and a pharmaceutical composition containing same. This compound can be an effective agent for the prophylaxis and treatment of the diseases curable based on a hypoglycemic action, and the diseases curable based on a cGMP-PDE inhibitory action, a smooth muscle relaxing action, a bronchodilating action, a vasodilating action, a smooth muscle cell inhibitory action and an allergy suppressing action.
Sulfonamide compounds and medicinal use thereof
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Page column 139, (2010/02/04)
A sulfonamide compound of the formula (I):R 1 --SO 2 NHCO--A--R 2 (I)wherein R 1 is alkyl, alkenyl, alkynyl and the like; A is an optionally substituted heteropolycyclic group except benzimidazolyl, indolyl, 4,7-dihydrobenzimidazolyl and 2,3-dihydrobenzoxazinyl; X is alkylene, oxa, oxa(lower)alkylene and the like; and R 2 is optionally substituted aryl, substituted biphenylyl and the like, a salt thereof and a pharmaceutical composition comprising the same. The sulfonamide compound is effective for the diseases treatable based on their blood sugar level-depressing activity, cGMP-PDE (especially PDE-V)-inhibiting activity, smooth muscle relaxing activity, bronchodilating activity, vasodilating activity, smooth muscle cell suppressing activity, and antiallergic activity.
