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CAS 850568-37-5

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[3-(ethoxycarbonyl)-5-nitrophenyl]boronic acid

Description:
[3-(Ethoxycarbonyl)-5-nitrophenyl]boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group, which is known for its ability to form reversible covalent bonds with diols, making it useful in various applications, including organic synthesis and medicinal chemistry. The compound features a nitrophenyl moiety, which contributes to its electronic properties and can enhance its reactivity. The ethoxycarbonyl group introduces an ester functionality, providing additional sites for chemical reactivity and potential interactions in biological systems. This compound is typically a solid at room temperature and may exhibit moderate solubility in organic solvents. Its boronic acid nature allows it to participate in Suzuki-Miyaura cross-coupling reactions, making it valuable in the synthesis of complex organic molecules. Additionally, the presence of the nitro group can influence the compound's polarity and reactivity, potentially affecting its biological activity and interactions with other molecules. Overall, [3-(ethoxycarbonyl)-5-nitrophenyl]boronic acid is a versatile compound with significant implications in synthetic and medicinal chemistry.
Formula:C9H10BNO6
InChI:InChI=1/C9H10BNO6/c1-2-17-9(12)6-3-7(10(13)14)5-8(4-6)11(15)16/h3-5,13-14H,2H2,1H3
SMILES:CCOC(=O)c1cc(cc(c1)N(=O)=O)B(O)O
Synonyms:
  • Benzoic Acid, 3-Borono-5-Nitro-, Ethyl Ester
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