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CAS 24341-76-2

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B-(2-Methyl-3,5-dinitrophenyl)boronic acid

Description:
B-(2-Methyl-3,5-dinitrophenyl)boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a substituted phenyl ring. This compound features a boron atom bonded to a phenyl group that is further substituted with two nitro groups and a methyl group, which significantly influences its chemical reactivity and properties. The presence of the boronic acid moiety allows for participation in various chemical reactions, including Suzuki coupling, which is valuable in organic synthesis. The nitro groups contribute to the compound's electron-withdrawing characteristics, enhancing its acidity and reactivity. Additionally, the methyl group can affect the steric and electronic properties of the molecule. B-(2-Methyl-3,5-dinitrophenyl)boronic acid is often utilized in research and development, particularly in the fields of medicinal chemistry and materials science, due to its ability to form complexes with diols and its potential applications in sensor technology. Safety precautions should be observed when handling this compound, as it may pose health risks due to its reactive nature and the presence of nitro groups.
Formula:C7H7BN2O6
InChI:InChI=1S/C7H7BN2O6/c1-4-6(8(11)12)2-5(9(13)14)3-7(4)10(15)16/h2-3,11-12H,1H3
InChI key:InChIKey=ZESXGHPFWNSQQV-UHFFFAOYSA-N
SMILES:B(O)(O)C1=C(C)C(N(=O)=O)=CC(N(=O)=O)=C1
Synonyms:
  • B-(2-Methyl-3,5-dinitrophenyl)boronic acid
  • Boronic acid, (2-methyl-3,5-dinitrophenyl)-
  • boronic acid, B-(2-methyl-3,5-dinitrophenyl)-
  • o-Tolueneboronic acid, 3,5-dinitro-
  • (2-Methyl-3,5-dinitrophenyl)boronic acid
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