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CAS 871329-54-3

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(4-tert-butyl-3-nitro-phenyl)boronic acid

Description:
(4-tert-butyl-3-nitro-phenyl)boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a phenyl ring that is further substituted with a tert-butyl group and a nitro group. This compound typically exhibits a white to off-white crystalline appearance and is soluble in polar organic solvents, such as methanol and ethanol, while being less soluble in non-polar solvents. The presence of the boronic acid group allows for participation in Suzuki-Miyaura cross-coupling reactions, making it valuable in organic synthesis, particularly in the formation of carbon-carbon bonds. The tert-butyl group contributes to the steric bulk, influencing the reactivity and selectivity in chemical reactions, while the nitro group can serve as a handle for further functionalization. Additionally, this compound may exhibit interesting electronic properties due to the electron-withdrawing nature of the nitro group, which can affect its reactivity and interactions in various chemical environments. Overall, (4-tert-butyl-3-nitro-phenyl)boronic acid is a versatile building block in synthetic organic chemistry.
Formula:C10H14BNO4
InChI:InChI=1/C10H14BNO4/c1-10(2,3)8-5-4-7(11(13)14)6-9(8)12(15)16/h4-6,13-14H,1-3H3
SMILES:CC(C)(C)c1ccc(cc1N(=O)=O)B(O)O
Synonyms:
  • (4-tert-Butyl-3-nitrophenyl)boronic acid
  • boronic acid, B-[4-(1,1-dimethylethyl)-3-nitrophenyl]-
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