CAS 29682-53-9: ethyl 5-methyl-1,2,3-thiadiazole-4-carboxylate

Description: Ethyl 5-methyl-1,2,3-thiadiazole-4-carboxylate is a heterocyclic organic compound characterized by its thiadiazole ring, which contains both sulfur and nitrogen atoms. This compound features a carboxylate functional group, contributing to its potential reactivity and solubility in polar solvents. The presence of the ethyl ester group enhances its lipophilicity, making it suitable for various applications in organic synthesis and potentially in agrochemical formulations. The methyl group at the 5-position of the thiadiazole ring can influence the compound's biological activity and stability. Ethyl 5-methyl-1,2,3-thiadiazole-4-carboxylate may exhibit interesting pharmacological properties, making it a subject of interest in medicinal chemistry. Its molecular structure allows for various chemical modifications, which can lead to derivatives with enhanced or altered properties. As with many thiadiazole derivatives, it may also possess antimicrobial or antifungal activities, although specific biological data would be necessary to confirm such effects. Overall, this compound represents a versatile building block in the field of organic chemistry.

Formula: C₆H₈N₂O₂S

InChI: InChI=1/C6H8N2O2S/c1-3-10-6(9)5-4(2)11-8-7-5/h3H2,1-2H3

Synonyms:

• 4-(Ethoxycarbonyl)-5-methyl-1,2,3-thiadiazole

1,2,3-Thiadiazole-4-carboxylic acid, 5-methyl-, ethyl ester

CAS: 29682-53-9

• Formula: C₆H₈N₂O₂S
• Molecular weight: 172.2049

5-Methyl-[1,2,3]thiadiazole-4-carboxylic acid ethyl ester

CAS: 29682-53-9

• Molecular weight: 172.20g/mol

5-Methyl-1,2,3-Thiadiazole-4-Carboxylic Acid Ethyl Ester

CAS: 29682-53-9

The 5-methyl-1,2,3-thiadiazole-4-carboxylic acid ethyl ester is a monomer that belongs to the amide class. It …

• Formula: C₆H₈N₂O₂S
• Purity: Min. 95%
• Molecular weight: 172.21 g/mol