CAS 438225-41-3
:4-ethyl-5-methylthiophene-3-carbohydrazide
Description:
4-Ethyl-5-methylthiophene-3-carbohydrazide is an organic compound characterized by its unique structure, which includes a thiophene ring, an ethyl group, a methyl group, and a hydrazide functional group. The presence of the thiophene ring imparts aromatic properties, contributing to its stability and potential reactivity. This compound is typically a solid at room temperature and may exhibit moderate solubility in organic solvents due to its hydrophobic thiophene moiety. The hydrazide functional group suggests potential for reactivity, particularly in forming hydrazones or participating in condensation reactions. Additionally, compounds like this may exhibit biological activity, making them of interest in pharmaceutical research. The specific arrangement of substituents on the thiophene ring can influence its electronic properties and reactivity, which are important for applications in materials science and medicinal chemistry. Overall, 4-ethyl-5-methylthiophene-3-carbohydrazide represents a versatile structure with potential applications in various chemical and biological fields.
Formula:C8H12N2OS
InChI:InChI=1/C8H12N2OS/c1-3-6-5(2)12-4-7(6)8(11)10-9/h4H,3,9H2,1-2H3,(H,10,11)
SMILES:CCc1c(C)scc1C(=NN)O
Synonyms:- 3-Thiophenecarboxylic Acid, 4-Ethyl-5-Methyl-, Hydrazide
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