40964-56-5 Usage
Uses
Used in Pharmaceutical Industry:
4-Bromo-1H-1,2,3-triazole is used as a pharmaceutical agent for its diverse therapeutic properties. It is recognized for its fungicidal, antimicrobial, antidepressant, antibacterial, anti-inflammatory, analgesic, and antitumor activities, which contribute to its potential use in developing treatments for various diseases and conditions.
Used in Antifungal Applications:
In the field of antifungal agents, 4-bromo-1H-1,2,3-triazole is utilized for its fungicidal properties, helping to combat fungal infections and contributing to the development of effective antifungal medications.
Used in Antimicrobial Applications:
4-Bromo-1H-1,2,3-triazole also serves as an antimicrobial agent, leveraging its ability to inhibit the growth of microorganisms, which is crucial in the creation of antibiotics and other antimicrobial drugs.
Used in Antidepressant Applications:
4-bromo-1H-1,2,3-triazole is used as an antidepressant agent, potentially aiding in the development of medications to treat depression and related mood disorders.
Used in Anti-inflammatory and Analgesic Applications:
4-Bromo-1H-1,2,3-triazole is employed for its anti-inflammatory and analgesic effects, making it a candidate for the development of drugs to alleviate pain and reduce inflammation.
Used in Antitumor Applications:
Lastly, 4-bromo-1H-1,2,3-triazole is used in antitumor applications, where its potential to combat tumor growth highlights its importance in the realm of oncology and the development of anticancer drugs.
Check Digit Verification of cas no
The CAS Registry Mumber 40964-56-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,0,9,6 and 4 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 40964-56:
(7*4)+(6*0)+(5*9)+(4*6)+(3*4)+(2*5)+(1*6)=125
125 % 10 = 5
So 40964-56-5 is a valid CAS Registry Number.
40964-56-5Relevant academic research and scientific papers
INTRODUCTION OF SUBSTITUENTS INTO 5-MEMBERED AZA-HETEROAROMATICS
Begtrup, Mikael
, p. 573 - 598 (2007/10/02)
With emphasis on mono- and regio-selectively, methods for introduction of substituents at nitrogen and carbon atoms of 5-membered aza-heteroaromatics have been developed.The methods involve application of activation and of assistant groups for direction and protection.Activation has been achieved by the use of quaternary azolium ions and azol-N-oxides as reactive intermediates.If necessary, the N-oxides were further activated by alkylation or acylation.
