1086376-35-3

Basic information

• Product Name: [5-(5-bromo-2-furyl)-2-oxo-1,3,4-oxadiazol-3(2h)-yl]acetic acid
• Synonyms: [5-(5-bromo-2-furyl)-2-oxo-1,3,4-oxadiazol-3(2h)-yl]acetic acid;[5-(5-Bromo-2-furyl)-2-oxo-1,3,4-oxadiazol-3(2H)-yl]acetic a
• CAS NO: 1086376-35-3
• Molecular Formula: C8H5BrN2O5
• Molecular Weight: 289.0397
• Product Categories: Furans, Benzofurans & Dihydrobenzofurans;Furans, Benzofurans & Dihydrobenzofurans;Halides
• Mol File: 1086376-35-3.mol
• Article Data: 0

Chemical Properties

• Appearance: /
• CAS DataBase Reference: [5-(5-bromo-2-furyl)-2-oxo-1,3,4-oxadiazol-3(2h)-yl]acetic acid(CAS DataBase Reference)
• NIST Chemistry Reference: [5-(5-bromo-2-furyl)-2-oxo-1,3,4-oxadiazol-3(2h)-yl]acetic acid(1086376-35-3)
• EPA Substance Registry System: [5-(5-bromo-2-furyl)-2-oxo-1,3,4-oxadiazol-3(2h)-yl]acetic acid(1086376-35-3)

Safety Data

• Hazardous Substances Data: 1086376-35-3(Hazardous Substances Data)

Usage

Description

[5-(5-Bromo-2-furyl)-2-oxo-1,3,4-oxadiazol-3(2H)-yl]acetic acid is a chemical compound belonging to the oxadiazole family, characterized by the presence of a furan ring and a carboxylic acid group. [5-(5-Bromo-2-furyl)-2-oxo-1,3,4-oxadiazol-3(2H)-yl]acetic acid has garnered interest due to its potential biological and pharmacological applications, making it a subject of study for various properties such as antiviral, antimicrobial, and anti-inflammatory activities.

Uses

Used in Pharmaceutical Research:
[5-(5-Bromo-2-furyl)-2-oxo-1,3,4-oxadiazol-3(2H)-yl]acetic acid is used as a compound in pharmaceutical research for its potential antiviral, antimicrobial, and anti-inflammatory properties. Its unique structure and properties make it a promising candidate for the development of new drugs and therapies.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, [5-(5-Bromo-2-furyl)-2-oxo-1,3,4-oxadiazol-3(2H)-yl]acetic acid is utilized as a key compound for exploring its potential therapeutic applications. Its structure offers opportunities for further modification and optimization to enhance its biological activities and pharmacological properties, contributing to the advancement of novel drug candidates.