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CAS 117342-20-8

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(3-Methoxycarbonyl-5-nitrophenyl)boronic acid

Description:
(3-Methoxycarbonyl-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. This compound features a nitrophenyl moiety, which contributes to its electronic properties and can enhance its reactivity. The methoxycarbonyl group introduces an ester functionality, providing additional sites for chemical modification. Typically, boronic acids exhibit moderate solubility in polar solvents, and their reactivity can be influenced by the substituents on the aromatic ring. This compound may be utilized in Suzuki coupling reactions, a key method for forming carbon-carbon bonds in organic synthesis. Its unique structural features make it a valuable intermediate in the development of pharmaceuticals and agrochemicals. As with many boronic acids, it is important to handle this compound with care, considering its potential reactivity and the need for appropriate storage conditions to maintain stability.
Formula:C8H8BNO6
InChI:InChI=1/C8H8BNO6/c1-16-8(11)5-2-6(9(12)13)4-7(3-5)10(14)15/h2-4,12-13H,1H3
SMILES:COC(=O)c1cc(cc(c1)N(=O)=O)B(O)O
Synonyms:
  • 3-Methoxycarbonyl-5-nitrophenylboronicacid
  • 3-(Methoxycarbonyl)-5-Nitrobenzeneboronic Acid
  • 3-Methoxycarbonyl-5-Nitrophenylboronic Acid
  • 3-METHOXYCARBONYL-5-NITROPHENYLBORONIC ACID 98%
  • 3-Methoxycarbonyl-5-Nitropheny
  • METHYL 3-BORONO-5-NITROBENZOATE
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