CAS 1348114-42-0

2-Thiophenecarboxylic acid, 5-amino-4-nitro-, ethyl ester

Description:

2-Thiophenecarboxylic acid, 5-amino-4-nitro-, ethyl ester is an organic compound characterized by its thiophene ring structure, which is a five-membered aromatic heterocycle containing sulfur. This compound features a carboxylic acid functional group, an amino group, and a nitro group, contributing to its reactivity and potential applications in pharmaceuticals and agrochemicals. The ethyl ester moiety enhances its solubility and bioavailability. Typically, compounds of this nature exhibit moderate to high polarity due to the presence of polar functional groups, which can influence their interaction with biological systems. The nitro group is known for its electron-withdrawing properties, which can affect the compound's acidity and reactivity. Additionally, the amino group can participate in hydrogen bonding, further influencing the compound's physical and chemical properties. Overall, 2-Thiophenecarboxylic acid, 5-amino-4-nitro-, ethyl ester is of interest for its potential biological activity and utility in synthetic organic chemistry.

Formula: C₇H₈N₂O₄S

Synonyms:

• 2-Thiophenecarboxylic acid, 5-amino-4-nitro-, ethyl ester

Ethyl 5-amino-4-nitrothiophene-2-carboxylate

CAS: 1348114-42-0

Ethyl 5-amino-4-nitrothiophene-2-carboxylate

Purity: 95%

Molecular weight: 216.22g/mol

Ref: 54-OR1047861