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CAS 25785-09-5

:

ethyl 5-nitro-1-benzothiophene-2-carboxylate

Description:
Ethyl 5-nitro-1-benzothiophene-2-carboxylate is a chemical compound characterized by its unique structure, which includes a benzothiophene ring fused with a nitro group and an ester functional group. This compound typically exhibits a yellow to orange color due to the presence of the nitro group, which can also influence its reactivity and solubility. It is generally soluble in organic solvents such as ethanol and dichloromethane, while being less soluble in water. The presence of the nitro group can impart electrophilic characteristics, making it a potential candidate for various chemical reactions, including nucleophilic substitutions. Ethyl 5-nitro-1-benzothiophene-2-carboxylate may also exhibit biological activity, which could be of interest in pharmaceutical research. Safety data should be consulted for handling and storage, as nitro compounds can be sensitive to heat and shock. Overall, this compound is significant in organic synthesis and may have applications in materials science and medicinal chemistry.
Formula:C11H9NO4S
InChI:InChI=1/C11H9NO4S/c1-2-16-11(13)10-6-7-5-8(12(14)15)3-4-9(7)17-10/h3-6H,2H2,1H3
SMILES:CCOC(=O)c1cc2cc(ccc2s1)N(=O)=O
Synonyms:
  • Benzo[b]thiophene-2-carboxylic acid, 5-nitro-, ethyl ester
  • Ethyl-5-nitro-1-benzothiophen-2-carboxylat
  • 5-Nitro-Benzo[B]Thiophene-2-Carboxylic Acid Ethyl Ester
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