CAS 23903-46-0

Ethyl 5-amino-4-cyano-3-methylthiophene-2-carboxylate

Description:

Ethyl 5-amino-4-cyano-3-methylthiophene-2-carboxylate is a chemical compound characterized by its unique structure, which includes a thiophene ring, an amino group, a cyano group, and an ester functional group. This compound typically appears as a solid or crystalline substance and is soluble in organic solvents, reflecting its polar and non-polar characteristics due to the presence of both hydrophilic (amino and carboxylate) and hydrophobic (thiophene and ethyl) components. The presence of the cyano group contributes to its reactivity, making it a potential candidate for various chemical reactions, including nucleophilic substitutions and cycloadditions. Ethyl 5-amino-4-cyano-3-methylthiophene-2-carboxylate may exhibit biological activity, which could be of interest in pharmaceutical research, particularly in the development of new drugs or agrochemicals. Safety data should be consulted for handling and storage, as with any chemical substance, to ensure proper precautions are taken.

Formula: C₉H₁₀N₂O₂S

InChI: InChI=1/C9H10N2O2S/c1-3-13-9(12)7-5(2)6(4-10)8(11)14-7/h3,11H2,1-2H3

SMILES: CCOC(=O)c1c(C)c(C#N)c(N)s1

Synonyms:

• 2-Thiophenecarboxylic acid, 5-amino-4-cyano-3-methyl-, ethyl ester
• 5-Amino-4-cyano-3-methyl-thiophene-2-carboxylic acid ethyl ester
• Thiophene-2-carboxylic acid, 5-amino-4-cyano-3-methyl-, ethyl ester

5-Amino-4-cyano-3-methyl-thiophene-2-carboxylic acid ethyl ester

CAS: 23903-46-0

Formula: C₉H₁₀N₂O₂S

Purity: 95.0%

Color and Shape: Solid

Molecular weight: 210.25

Ref: 10-F030609

Ethyl 5-amino-4-cyano-3-methylthiophene-2-carboxylate

CAS: 23903-46-0

Ethyl 5-amino-4-cyano-3-methylthiophene-2-carboxylate is an organic compound that belongs to the family of oxadiazoles. It has been shown to be highly active against gram-negative bacteria such as Pseudomonas aeruginosa and Serratia marcescens, and also has antibacterial activity against Staphylococcus aureus. This compound may have neuroprotective effects in rats with Alzheimer's disease due to its ability to inhibit peroxide release from neutrophils. Ethyl 5-amino-4-cyano-3-methylthiophene-2-carboxylate also inhibits bacterial DNA gyrase and topoisomerase IV, enzymes which maintain the structural integrity of bacterial DNA. This inhibition leads to DNA damage, leading to cell death by inhibiting the production of proteins vital for cell division.

Formula: C₉H₁₀N₂O₂S

Purity: Min. 95%

Molecular weight: 210.25 g/mol

Ref: 3D-FE113367