13182-73-5

Usage

Explanation

The molecular formula represents the number of atoms of each element present in a molecule. In this case, the compound has 8 carbon atoms, 6 hydrogen atoms, 1 chlorine atom, 5 nitrogen atoms, and 1 sulfur atom.

Explanation

The compound belongs to a class of chemical compounds known as triazolo-thiadiazoles, which are characterized by the presence of a triazole and a thiadiazole ring fused together.

Explanation

The compound has an amine group (-NH2) and a chlorophenyl group (C6H4Cl) attached to its structure, which contribute to its unique properties and potential applications.

Explanation

Due to its unique structure and potential biological activities, the compound may be useful in the development of new drugs and therapies. However, further research is needed to fully understand its properties and potential uses.

Explanation

As a relatively new and complex chemical compound, more research is required to determine its specific properties, such as solubility, stability, and reactivity, as well as its potential applications in various fields, including medicine and pharmaceuticals.

Chemical class

Triazolo-thiadiazole derivative

Structure

Contains an amine group and a chlorophenyl substituent

Potential applications

Pharmaceutical research and drug development

Need for further study

Properties and potential uses

Upstream product

• 506-68-3 bromocyane 
• 13229-02-2 4-amino-5-(2-chlorophenyl)-2,4-dihydro-3H[1,2,4]triazole-3-thione 
• 13229-02-2 4-amino-5-(2-chlorophenyl)-4H-1,2,4-triazole-3-thiol 

Relevant academic research and scientific papers

Synthesis, characterization and fungitoxicity of 3,4,6-triayl-striazolo [3,4-b]-1,3,4-thiadiazolo [1,3,5]-triazine-5-thiones

In the present work 3,4,6-triayl-s-triazolo [3,4-b]-1,3,4-thiadiazolo [1,3,50-triazine-5-thiones (IVan) were synehsized by 4+2 cycloaddition of 6-arylidine amino-3-aryl-s-triazolo [3,4-b]-1,3,4-thiadiazoles (IIIa-n) are arylisothiocynate in dry tolune as solvent. 6-Arylidine amino-3-aryl-s-triazolo [3,4-b]-1,3,4-thiadiazoles (IIIa-n) were prepared from aromatic aldehyde refluxing in absolute ethanol with 6-amino-3-aryl-s-triazole [3,4-b]-1,3,4-thiadiazoles (IIa-g), which are prepared from 3-aryl, 4-amino-5-mercaptos-triazole (Ia-g) by treating it with cyanogen bromide in ethanol. Starting material 3-aryl, 4-amino-5-mercapto-s-triazoles (Ia-g) wre prepred in excellent yield following the method of Ried and Heindel1. The reaction sequence leading to the formation of titled compounds are given in the scheme 1. All the synthesized fourteen titled compounds were well characterized by their analytical and spectral data. Fungitoxicity of titled compounds (IVa-n) have been evaluated against two fungal species i.e. Helminthosporium orayzee and Alternaria solanai.

Synthesis of Heterocycles. Part VII . Synthesis and Antimicrobial Activity of Some 7H-s-Triazolothiadiazine and s-Triazolothiadiazole Derivatives

The cyclization of 4-amino-5-aryl-3-cyanomethylthio-1,2,4-triazoles II in the presence of concentrated sulfuric acid yields 7H-6-amino-s-triazolothiadiazines III.Cyclization of 4-amino-5-aryl-1,2,4-triazole-3-thiones I with phenacyl chloride yields 7H-3-aryl-6-phenyl-s-triazolothiadiazines IV.Similarly, compounds I condensed with cyanogen bromide, phenyl isothiocyanate and carbon disulfide to give the corresponding cyclized products 6-amino-3-aryl-s-triazolothiadiazoles V, 3-aryl-6-phenylamino-s-triazolothiadiazoles VI and 3-aryl-s-triazolothiadiazol-6(5H)thiones VII, respectively.Also in the presence of phosphoryl chloride, compounds I underwent cyclization with monocarboxylic acids and oxalic acid to 3,6-diaryl-s-triazolothiadiazole VIII and 6,6'-bis(3-aryl-s-triazolothiadiazoles) IX.The above compounds were screened for their antimicrobial activity.