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1,3,4-Thiadiazol-2(3H)-one, 5-(phenylamino)-, hydrazone is a complex organic compound with the chemical formula C9H8N4OS. It is derived from the parent compound 1,3,4-thiadiazol-2(3H)-one, which is a heterocyclic molecule containing sulfur, nitrogen, and oxygen atoms. The 5-(phenylamino)- derivative introduces a phenylamine group to the molecule, while the hydrazone functional group is formed by the condensation of the carbonyl group with a hydrazine molecule. 1,3,4-Thiadiazol-2(3H)-one, 5-(phenylamino)-, hydrazone is of interest in the field of organic chemistry and may have potential applications in the synthesis of pharmaceuticals, agrochemicals, or other specialty chemicals. Its specific properties, reactivity, and potential uses would depend on its molecular structure and the context in which it is being studied or applied.

5319-81-3

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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.
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