957760-15-5 Usage
Uses
Used in Pharmaceutical Industry:
7-chloro-1-Methyl-1H-pyrazolo[3,4-c]pyridine serves as a valuable building block in the synthesis of a range of drugs and bioactive compounds. Its unique structure allows for the development of new pharmaceutical agents with diverse therapeutic applications.
Used in Antifungal and Antibacterial Agents:
Due to its inherent biological activities, 7-chloro-1-Methyl-1H-pyrazolo[3,4-c]pyridine is utilized as an antifungal and antibacterial agent. It can be incorporated into formulations to combat various fungal and bacterial infections, contributing to the development of novel treatments in the medical field.
Used in Agrochemical Development:
7-chloro-1-Methyl-1H-pyrazolo[3,4-c]pyridine's potential extends to the agrochemical industry, where it may be employed in the development of new pesticides or other agrochemicals. Its unique structure and properties could lead to the creation of innovative products that enhance crop protection and yield.
Used in Research and Development:
7-chloro-1-Methyl-1H-pyrazolo[3,4-c]pyridine is also used in research settings to explore its full potential and understand its benefits in various applications. Further studies are necessary to uncover its capabilities and optimize its use in different industries.
Check Digit Verification of cas no
The CAS Registry Mumber 957760-15-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,5,7,7,6 and 0 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 957760-15:
(8*9)+(7*5)+(6*7)+(5*7)+(4*6)+(3*0)+(2*1)+(1*5)=215
215 % 10 = 5
So 957760-15-5 is a valid CAS Registry Number.
957760-15-5Relevant academic research and scientific papers
Zhang, Yan,Ye, Wei,Wang, Haisheng,Schneller, Stewart W.
, p. 723 - 730 (2012)
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.
