CAS 50483-82-4
:3-phenyl-1,2,4-thiadiazole
Description:
3-Phenyl-1,2,4-thiadiazole is an organic compound characterized by its unique heterocyclic structure, which includes a thiadiazole ring fused with a phenyl group. This compound features a five-membered ring containing two nitrogen atoms and one sulfur atom, contributing to its distinct chemical properties. It is typically a solid at room temperature and may exhibit a range of colors depending on its purity and specific form. The presence of the phenyl group enhances its aromatic characteristics, potentially influencing its reactivity and solubility in various solvents. 3-Phenyl-1,2,4-thiadiazole is of interest in various fields, including materials science and medicinal chemistry, due to its potential applications in organic electronics, as well as its biological activity. The compound may exhibit properties such as fluorescence or photostability, making it suitable for use in dyes or sensors. As with many thiadiazole derivatives, it may also possess antimicrobial or antifungal properties, although specific biological activities can vary widely based on structural modifications and substituents.
Formula:C8H6N2S
InChI:InChI=1/C8H6N2S/c1-2-4-7(5-3-1)8-9-6-11-10-8/h1-6H
SMILES:c1ccc(cc1)c1ncsn1
Synonyms:- 3-PHENYL-1,2,4-THIADIAZOLE
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Found 1 products.
3-Phenyl-1,2,4-thiadiazole
CAS:<p>3-Phenyl-1,2,4-thiadiazole is a tricyclic compound that has been synthesized in equimolar amounts by reactions of benzene with sulfur and nitric acid. This substance has also been shown to react with a number of other compounds and produce adducts. The reaction of 3-phenyl-1,2,4-thiadiazole with potassium bromide produces an adduct that contains the reactive benzylic bromide ion (3’). 3-Phenyl-1,2,4-thiadiazole is used in organic chemistry as a reagent for the synthesis of dithioesters. It can also be used to study the photochemistry of benzonitrile derivatives.</p>Formula:C8H6N2SPurity:Min. 95%Molecular weight:162.21 g/mol
