120107-40-6

Usage

Heterocyclic compound

The compound contains a five-membered ring with different types of atoms (heteroatoms), making it a heterocyclic compound.

Five-membered ring structure

The ring is composed of one oxygen atom, two nitrogen atoms, and two carbon atoms.

Potential biological and pharmaceutical properties

The compound has been studied for its possible applications in medicine and pharmaceuticals due to its unique structure and properties.

Antifungal and antibacterial agent

The compound has shown the ability to inhibit the growth of fungi and bacteria, making it a potential candidate for treating infections.

Anti-inflammatory and analgesic properties

The compound has demonstrated the potential to reduce inflammation and relieve pain, which could be beneficial in treating various inflammatory and painful conditions.

Promising candidate for further research and development

Due to its structure and properties, the compound is considered a valuable subject for additional research and development in the field of medicinal chemistry.

Upstream product

• 1904-58-1 anthranilic acid hydrazide 
• 74-11-3 para-chlorobenzoic acid 
• 134-20-3 2-carbomethoxyaniline 

Relevant academic research and scientific papers

Comparison between antioxidant activity of 2,5-disubstituted 1,3,4-oxadiazoles containing heteroaromatic ring and aromatic ring at 2nd position

A series of 4-[5-(substitutedphenyl)-1,3,4-oxadiazol- 2-yl]-pyridine) and 2-[5-substitutedphenyl)-1,3,4- oxadiazol-2-yl]-benzenamine derivatives were synthesized from substituted esters and hydrazine hydrate in the presence of ethanol to give isonicotinic acid hydrazide and 2-aminobenzohydrazide followed by reaction with phosphorus oxychloride and various aromatic acids. All the compounds were tested for their in vitro antioxidant activity by 1,1-diphenyl-2-picryl hydrazyl (DPPH) method. Compounds containing aromatic group at 2nd position showed significant activity as compared to standard (ascorbic acid) which concludes that the presence of aromatic group increases the free radical scavenging activity. Springer Science+Business Media, LLC 2010.

Reaction of 2-Aminobenzoylhydrazines with Carboxylic Acids: Formation of Quinazolin-4(3H)-one, 1,3,4-Oxadiazole and 1,3,4-Benzotriazepin-5-one Derivatives

Reactions of 2-aminobenzoylhydrazines with aliphatic acids give 1-(2'-acylaminobenzoyl)-2-acylhydrazines (4) which are cyclised to 3-amino-2-alkylquinazolin-4(3H)-ones (6).Aromatic acids react with 2-aminobenzoylhydrazines to give a mixture of 1-(2'-amino