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CAS 70799-12-1

:

{4-[(Dimethylamino)methyl]phenyl}boronic acid

Description:
{4-[(Dimethylamino)methyl]phenyl}boronic acid, with the CAS number 70799-12-1, 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 dimethylamino group. This compound typically exhibits properties such as being a white to off-white solid at room temperature, with solubility in polar solvents like water and alcohols due to the boronic acid moiety. It is known for its ability to form reversible covalent bonds with diols, making it useful in various applications, including organic synthesis, medicinal chemistry, and as a reagent in the development of sensors. The dimethylamino group enhances its nucleophilicity and can influence its reactivity and interaction with biological systems. Additionally, boronic acids are often utilized in cross-coupling reactions, such as Suzuki-Miyaura coupling, which is significant in the formation of carbon-carbon bonds in organic synthesis. Overall, this compound is valuable in both research and industrial applications due to its unique chemical properties.
Formula:C9H14BNO2
InChI:InChI=1/C9H14BNO2/c1-11(2)7-8-3-5-9(6-4-8)10(12)13/h3-6,12-13H,7H2,1-2H3
SMILES:CN(C)Cc1ccc(cc1)B(O)O
Synonyms:
  • boronic acid, B-[4-[(dimethylamino)methyl]phenyl]-
  • 4-((Dimethylamino)methyl)phenylboronic acid hydrochloride
  • 4-[(Dimethylamino)Methyl]Phenylboronic Acid
  • B-[4-[(Dimethylamino)methyl]phenyl]boronic acid
  • Boronic acid, B-[4-[(diMethylaMino)Methyl]phenyl]- hydrochloride
  • [4-[(Dimethylamino)methyl]phenyl]boronic acid 97%
  • {4-[(dimethylamino)methyl]phenyl}boronic acid(SALTDATA: FREE)
  • AKOS BRN-0614
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