16013-07-3 Usage
Description
3-(4-BROMOPHENYL)-1,2,4-OXADIAZOLE, with the molecular formula C8H5BrN2O, is a heterocyclic organic compound characterized by the presence of an oxadiazole ring fused with a bromophenyl group. 3-(4-BROMOPHENYL)-1,2,4-OXADIAZOLE is known for its intriguing biological and pharmacological properties, making it a valuable entity in the realms of medicinal chemistry and drug development.
Uses
Used in Medicinal Chemistry and Drug Development:
3-(4-BROMOPHENYL)-1,2,4-OXADIAZOLE is utilized as a key intermediate in the synthesis of pharmaceuticals due to its potential to modulate biological activities, offering a promising avenue for the creation of new therapeutic agents.
Used in Antimicrobial Agents:
In the field of antimicrobial chemistry, 3-(4-BROMOPHENYL)-1,2,4-OXADIAZOLE is used as an antimicrobial agent for its ability to combat various microorganisms, thereby serving in the development of new antibiotics and antifungal drugs.
Used in Anti-Inflammatory Agents:
3-(4-BROMOPHENYL)-1,2,4-OXADIAZOLE is employed as an anti-inflammatory agent, leveraging its pharmacological properties to mitigate inflammation, which is crucial in treating a range of conditions characterized by inflammatory responses.
Used in Material Science and Polymer Development:
Within material science, 3-(4-BROMOPHENYL)-1,2,4-OXADIAZOLE is used as a component in the development of new materials and polymers, capitalizing on its chemical structure to enhance material properties such as stability, reactivity, or specific interactions.
Used in Biological Imaging and Diagnostics:
3-(4-BROMOPHENYL)-1,2,4-OXADIAZOLE is used as a fluorescent probe in biological imaging and diagnostic applications, taking advantage of its optical properties to visualize cellular and molecular processes, aiding in the advancement of medical diagnostics and research.
Check Digit Verification of cas no
The CAS Registry Mumber 16013-07-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,0,1 and 3 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 16013-07:
(7*1)+(6*6)+(5*0)+(4*1)+(3*3)+(2*0)+(1*7)=63
63 % 10 = 3
So 16013-07-3 is a valid CAS Registry Number.
InChI:InChI=1/C8H5BrN2O/c9-7-3-1-6(2-4-7)8-10-5-12-11-8/h1-5H
16013-07-3Relevant articles and documents
NOVEL ARYL OR HETEROARYL TRIAZOLONE DERIVATIVES OR SALTS THEREOF, OR PHARMACEUTICAL COMPOSITIONS COMPRISING THE SAME
-
, (2019/10/15)
The present technology provides aryl or heteroaryl triazolone derivatives or pharmaceutically acceptable salts thereof, preparation processes thereof, pharmaceutical compositions comprising the same, and the use thereof. The aryl or heteroaryl triazolone derivatives or their pharmaceutically acceptable salts exhibit selective inhibitory activity on VAP-1 and therefore can be usefully applied, e.g., for the treatment and prophylaxis of nonalcoholic hepatosteatosis (NASH).
Microwave promoted one-pot synthesis of 2-aryl substituted 1,3,4-oxadiazoles and 1,2,4-oxadiazole derivatives using Al3+-K10 clay as a heterogeneous catalyst
Suresh, Dhanusu,Kanagaraj, Kuppusamy,Pitchumani, Kasi
supporting information, p. 3678 - 3682 (2014/06/23)
An efficient, inexpensive method is developed for the one-pot synthesis of 2-aryl substituted 1,3,4-oxadiazoles and 1,2,4-oxadiazoles starting from acid hydrazides and trimethyl orthoformate under solvent-free, microwave conditions using a reusable Alsup
