1373333-62-0 Usage
Description
7-chloro-2-Methyl-2H-pyrazolo[3,4-c]pyridine is a heterocyclic chemical compound characterized by a molecular formula of C8H6ClN3. It features a pyrazole ring fused to a pyridine ring, with a chlorine atom at the 7th position. This unique structure endows it with potential biological activities, making it a valuable compound in pharmaceutical research and drug development.
Uses
Used in Pharmaceutical Research and Drug Development:
7-chloro-2-Methyl-2H-pyrazolo[3,4-c]pyridine is utilized as a key intermediate in the synthesis of potential therapeutic agents. Its unique structure allows for the development of new drugs with specific target profiles, offering promising applications in the treatment of various diseases.
Used in Cancer Treatment:
In the field of oncology, 7-chloro-2-Methyl-2H-pyrazolo[3,4-c]pyridine is studied for its potential application in treating various types of cancer. Its unique chemical structure may enable the development of targeted therapies that can selectively affect cancer cells, reducing side effects and improving patient outcomes.
Used in Neurological Disorders Treatment:
7-chloro-2-Methyl-2H-pyrazolo[3,4-c]pyridine is also being investigated for its potential role in the treatment of neurological disorders. Its unique structure may allow for the development of drugs that can cross the blood-brain barrier, providing targeted treatment for conditions such as Alzheimer's disease, Parkinson's disease, and multiple sclerosis.
Used in Antimicrobial Applications:
7-chloro-2-Methyl-2H-pyrazolo[3,4-c]pyridine has been studied for its potential antimicrobial properties. Its unique structure may contribute to the development of new antibiotics or antifungal agents, addressing the growing issue of antibiotic resistance and providing alternative treatment options for various infections.
Used in Anti-Fungal Applications:
Similarly, 7-chloro-2-Methyl-2H-pyrazolo[3,4-c]pyridine is being explored for its potential antifungal properties. Its unique chemical structure may enable the development of new antifungal agents, offering effective treatment options for fungal infections and combating the increasing prevalence of drug-resistant fungal strains.
Check Digit Verification of cas no
The CAS Registry Mumber 1373333-62-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,7,3,3,3 and 3 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1373333-62:
(9*1)+(8*3)+(7*7)+(6*3)+(5*3)+(4*3)+(3*3)+(2*6)+(1*2)=150
150 % 10 = 0
So 1373333-62-0 is a valid CAS Registry Number.
1373333-62-0Relevant articles and documents
Carbocyclic 4-deazaformycins
Zhang, Yan,Ye, Wei,Wang, Haisheng,Schneller, Stewart W.
experimental part, p. 723 - 730 (2012/04/10)
The preparation of carbocyclic 4-deazaformycin and its 5-homoanalogue from a common vinyl precursor, and its N-1 and N-2 methyl derivatives is reported. The syntheses began with a highly stereoselective SN2 reaction between lithio 4-picolines and a protected 2,3-dihydroxy-4-vinylcyclopentyl triflate. The requisite fused pyrazole ring was created by an intramolecular diazonium reaction that was followed by vinyl transformation into the hydroxymethyl and the hydroxyethyl groups. The N-methyl derivatives arose by standard methylation conditions and the resultant N-Me regiochemistry was assigned by homo- and heteronuclear NMR spectroscopy. Georg Thieme Verlag Stuttgart · New York.
