CAS 18212-20-9
:Ethyl 4-methyl-1,2,3-thiadiazole-5-carboxylate
Description:
Ethyl 4-methyl-1,2,3-thiadiazole-5-carboxylate is an organic compound characterized by its thiadiazole ring, which incorporates sulfur and nitrogen atoms, contributing to its unique chemical properties. This compound features an ethyl ester functional group, which enhances its solubility in organic solvents and may influence its reactivity. The presence of the methyl group at the 4-position of the thiadiazole ring can affect the compound's steric and electronic properties, potentially impacting its biological activity and interactions with other molecules. Ethyl 4-methyl-1,2,3-thiadiazole-5-carboxylate is often studied for its potential applications in pharmaceuticals, agrochemicals, and as a building block in organic synthesis. Its CAS number, 18212-20-9, allows for easy identification in chemical databases. As with many thiadiazole derivatives, it may exhibit interesting biological activities, making it a subject of interest in medicinal chemistry and related fields. Proper handling and safety measures should be observed, as with all chemical substances, to mitigate any potential hazards associated with its use.
Formula:C6H8N2O2S
InChI:InChI=1/C6H8N2O2S/c1-3-10-6(9)5-4(2)7-8-11-5/h3H2,1-2H3
SMILES:CCOC(=O)c1c(C)nns1
Synonyms:- 4-Methyl-1,2,3-thiadiazole-5-carboxylic acid ethyl ester
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Found 3 products.
1,2,3-Thiadiazole-5-carboxylic acid, 4-methyl-, ethyl ester
CAS:Formula:C6H8N2O2SPurity:97%Color and Shape:LiquidMolecular weight:172.2049Ethyl 4-methyl-1,2,3-thiadiazole-5-carboxylate
CAS:Ethyl 4-methyl-1,2,3-thiadiazole-5-carboxylatePurity:≥95%Molecular weight:172.20g/mol4-Methyl-[1,2,3]thiadiazole-5-carboxylic acid ethyl ester
CAS:Formula:C6H8N2O2SPurity:98%Molecular weight:172.2


