CAS 1457-93-8
:5-methyl-2,1,3-benzothiadiazole
Description:
5-Methyl-2,1,3-benzothiadiazole is a heterocyclic compound characterized by its benzothiadiazole core, which consists of a benzene ring fused to a thiadiazole ring. This compound features a methyl group at the 5-position of the benzothiadiazole structure, influencing its chemical properties and reactivity. It is typically a crystalline solid with a relatively low solubility in water but may dissolve in organic solvents. The presence of the thiadiazole moiety imparts unique electronic properties, making it of interest in various applications, including organic electronics, photoconductors, and as a potential building block in the synthesis of more complex organic materials. Additionally, its structure may exhibit fluorescence, which can be advantageous in certain applications. The compound is also studied for its potential biological activities, although specific interactions and effects would require further investigation. Safety data should be consulted to understand its handling and toxicity, as with any chemical substance.
Formula:C7H6N2S
InChI:InChI=1/C7H6N2S/c1-5-2-3-6-7(4-5)9-10-8-6/h2-4H,1H3
SMILES:Cc1ccc2c(c1)nsn2
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Found 4 products.
2,1,3-Benzothiadiazole, 5-methyl-
CAS:Formula:C7H6N2SPurity:%Color and Shape:LiquidMolecular weight:150.20095-Methyl-2,1,3-benzothiadiazole
CAS:5-Methyl-2,1,3-benzothiadiazoleFormula:C7H6N2SPurity:≥95%Color and Shape:PowderMolecular weight:150.20g/mol5-Methylbenzo-2,1,3-thiadiazole
CAS:Formula:C7H6N2SPurity:95.0%Color and Shape:SolidMolecular weight:150.25-Methylbenzo[c][1,2,5]thiadiazole
CAS:<p>5-Methylbenzo[c][1,2,5]thiadiazole is a chemical compound that belongs to the group of mixtures. It is a yellow solid that can be purified by recrystallization from water and ethanol. This compound is soluble in alcohol, chloroform and ether. 5-Methylbenzo[c][1,2,5]thiadiazole has been shown to be an oxidizing agent when mixed with potassium permanganate or potassium perchlorate. The reactivity of this substance can also be seen when it reacts with chlorine gas to form the corresponding thiocarbonyl chloride. 5-Methylbenzo[c][1,2,5]thiadiazole has not been found to have any commercial applications at this time.</p>Formula:C7H6N2SPurity:Min. 95%Molecular weight:150.2 g/mol



