CAS 42783-04-0
:3-Thiophenecarboxylic acid, 2-amino-5-nitro-, ethyl ester
Description:
3-Thiophenecarboxylic acid, 2-amino-5-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, making it suitable for various chemical reactions and biological interactions. The presence of the nitro group typically imparts electron-withdrawing properties, influencing the compound's acidity and reactivity. Additionally, the amino group can participate in hydrogen bonding and nucleophilic reactions, further expanding its utility in synthetic chemistry. Overall, this compound's unique combination of functional groups and heterocyclic structure makes it a valuable candidate for research in medicinal chemistry and materials science. Safety and handling precautions should be observed due to the potential hazards associated with nitro compounds and their derivatives.
Formula:C7H8N2O4S
InChI:InChI=1S/C7H8N2O4S/c1-2-13-7(10)4-3-5(9(11)12)14-6(4)8/h3H,2,8H2,1H3
InChI key:InChIKey=UXDKVBJDZDRIKL-UHFFFAOYSA-N
SMILES:C(OCC)(=O)C=1C=C(N(=O)=O)SC1N
Synonyms:- 2-Amino-3-ethoxycarbonyl-5-nitrothiophene
- 3-Thiophenecarboxylic Acid, 2-Amino-5-Nitro-, Ethyl Ester
- Ethyl 2-amino-5-nitro-3-thenoate
- Ethyl 2-amino-5-nitro-3-thiophenecarboxylate
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