CymitQuimica logo

CAS 851756-54-2

:

(2,6-dichloro-3-methyl-phenyl)boronic acid

Description:
(2,6-Dichloro-3-methyl-phenyl)boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a phenyl ring that is substituted with two chlorine atoms and a methyl group. This compound typically exhibits properties such as being a white to off-white solid at room temperature, with moderate solubility in polar solvents like water and alcohols due to the boronic acid group. It is known for its utility in organic synthesis, particularly in cross-coupling reactions, such as Suzuki-Miyaura coupling, which is essential for forming carbon-carbon bonds. The presence of the chlorine substituents can influence its reactivity and electronic properties, making it a valuable intermediate in the synthesis of pharmaceuticals and agrochemicals. Additionally, boronic acids are known for their ability to form reversible complexes with diols, which can be exploited in various applications, including sensor technology and drug delivery systems. Safety precautions should be taken when handling this compound, as with many organoboron compounds, due to potential toxicity and environmental concerns.
Formula:C7H7BCl2O2
InChI:InChI=1/C7H7BCl2O2/c1-4-2-3-5(9)6(7(4)10)8(11)12/h2-3,11-12H,1H3
SMILES:Cc1ccc(c(c1Cl)B(O)O)Cl
Synonyms:
  • (2,6-Dichloro-3-methylphenyl)boronic acid
  • boronic acid, B-(2,6-dichloro-3-methylphenyl)-
Sort by
Purity (%)
0
100
|
0
|
50
|
90
|
95
|
100
Found 3 products.