35235-72-4 Usage
Uses
Used in Pharmaceutical Industry:
5-Chloro-[1,2,3,4]tetrazolo[1,5-a]pyridine is used as a key intermediate in the synthesis of various pharmaceutical drugs and agrochemicals, leveraging its wide range of biological activities for the development of new therapeutic agents.
Used in Antiviral, Antibacterial, and Antifungal Applications:
CTP is utilized for its antiviral, antibacterial, and antifungal properties, serving as a component in the formulation of treatments targeting a variety of infectious diseases.
Used in Epilepsy, Pain, and Inflammation Treatment:
5-Chloro-[1,2,3,4]tetrazolo[1,5-a]pyridine is studied for its potential applications in the treatment of neurological conditions such as epilepsy, as well as in managing pain and inflammation, due to its demonstrated biological effects in these areas.
Used in Medicinal and Agricultural Chemistry:
CTP is employed as a versatile building block in the synthesis of diverse compounds, contributing to the advancement of both medicinal and agricultural chemistry by enabling the creation of new chemical entities with potential applications in these fields.
Check Digit Verification of cas no
The CAS Registry Mumber 35235-72-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,5,2,3 and 5 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 35235-72:
(7*3)+(6*5)+(5*2)+(4*3)+(3*5)+(2*7)+(1*2)=104
104 % 10 = 4
So 35235-72-4 is a valid CAS Registry Number.
35235-72-4Relevant academic research and scientific papers
Reaction of N-fluoropyridinium fluoride with isonitriles and TMSN 3: A convenient one-pot synthesis of tetrazol-5-yl pyridines
Kiselyov, Alexander S.
, p. 4851 - 4854 (2007/10/03)
Reaction of N-fluoropyridinium fluoride generated in situ with a series of isonitriles and TMSN3 led to the formation of the corresponding tetrazol-5-yl pyridines in good yields (37-84%). A similar reaction sequence for quinoline yielded the respective derivatives of 2-quinoline. The proposed reaction mechanism involves the intermediate formation of a highly reactive carbene species.
