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CAS 20699-86-9

:

methyl 5-nitro-1-benzothiophene-2-carboxylate

Description:
Methyl 5-nitro-1-benzothiophene-2-carboxylate is an organic compound characterized by its unique structure, which includes a benzothiophene ring, a nitro group, and a carboxylate ester functional group. The presence of the nitro group typically imparts significant polarity and can influence the compound's reactivity, making it a potential candidate for various chemical reactions, including electrophilic substitutions. The benzothiophene moiety contributes to the compound's aromatic properties, which can enhance stability and influence solubility in organic solvents. As an ester, it may also exhibit typical ester reactivity, such as hydrolysis under acidic or basic conditions. This compound is of interest in synthetic organic chemistry and may have applications in pharmaceuticals or agrochemicals due to its structural features. Safety and handling precautions should be observed, as nitro compounds can be hazardous. Overall, methyl 5-nitro-1-benzothiophene-2-carboxylate is a versatile compound with potential applications in various fields of chemistry.
Formula:C10H7NO4S
InChI:InChI=1/C10H7NO4S/c1-15-10(12)9-5-6-4-7(11(13)14)2-3-8(6)16-9/h2-5H,1H3
SMILES:COC(=O)c1cc2cc(ccc2s1)N(=O)=O
Synonyms:
  • Benzo[B]Thiophene-2-Carboxylic Acid, 5-Nitro-, Methyl Ester
  • Methyl-5-nitro-1-benzothiophen-2-carboxylat
  • 5-Nitrobenzo[B]Thiophene-2-Carboxylate
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