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.
Check Digit Verification of cas no
The CAS Registry Mumber 120107-40-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,0,1,0 and 7 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 120107-40:
(8*1)+(7*2)+(6*0)+(5*1)+(4*0)+(3*7)+(2*4)+(1*0)=56
56 % 10 = 6
So 120107-40-6 is a valid CAS Registry Number.
120107-40-6Relevant articles and documents
Comparison between antioxidant activity of 2,5-disubstituted 1,3,4-oxadiazoles containing heteroaromatic ring and aromatic ring at 2nd position
Maheshwari, Radhika,Chawla, Pooja,Saraf, Shubhini A.
experimental part, p. 1650 - 1655 (2012/06/15)
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.
