5319-81-3 Usage
Chemical Structure
1,3,4-Thiadiazol-2(3H)-one, 5-(phenylamino)-, hydrazone is a chemical compound with a thiadiazole ring and a hydrazone functional group attached to it.
Family
It belongs to the thiadiazole family of compounds.
Potential Medicinal Properties
1,3,4-Thiadiazol-2(3H)-one, 5-(phenylamino)-, hydrazone has potential medicinal properties and has been studied for its anti-inflammatory, antimicrobial, and anticancer activities.
Pharmacophore
It has been identified as a potential pharmacophore for the design of novel bioactive molecules.
Drug Discovery and Development
The compound has attracted attention in the field of drug discovery and development due to its potential medicinal properties.
Research Focus
Research on 1,3,4-Thiadiazol-2(3H)-one, 5-(phenylamino)-, hydrazone has primarily focused on its anti-inflammatory, antimicrobial, and anticancer activities.
Promising Candidate
It is considered a promising candidate for further investigation in the search for new medical treatments.
Molecular Weight
The molecular weight of 1,3,4-Thiadiazol-2(3H)-one, 5-(phenylamino)-, hydrazone is approximately 217.25 g/mol.
Appearance
It is typically found as a solid substance.
Solubility
The solubility of 1,3,4-Thiadiazol-2(3H)-one, 5-(phenylamino)-, hydrazone in various solvents is not explicitly mentioned in the provided material, but it is generally expected to be more soluble in polar solvents due to its polar functional groups.
Stability
The stability of 1,3,4-Thiadiazol-2(3H)-one, 5-(phenylamino)-, hydrazone under different conditions is not specified in the material, but it is generally expected to be stable under normal laboratory conditions.
Synthesis
The synthesis of 1,3,4-Thiadiazol-2(3H)-one, 5-(phenylamino)-, hydrazone involves the formation of a thiadiazole ring and subsequent attachment of a hydrazone functional group to the 5-position of the phenylamino group.
Applications
The primary applications of 1,3,4-Thiadiazol-2(3H)-one, 5-(phenylamino)-, hydrazone are in the field of medicinal chemistry, specifically in the development of new drugs with potential anti-inflammatory, antimicrobial, and anticancer properties.
Check Digit Verification of cas no
The CAS Registry Mumber 5319-81-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,3,1 and 9 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 5319-81:
(6*5)+(5*3)+(4*1)+(3*9)+(2*8)+(1*1)=93
93 % 10 = 3
So 5319-81-3 is a valid CAS Registry Number.