CAS 1334226-27-5

B-[3-[(Methylphenylamino)methyl]phenyl]boronic acid

Description:

B-[3-[(Methylphenylamino)methyl]phenyl]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. This compound features a phenyl ring substituted with a methylphenylamino group, enhancing its potential for biological activity and applications in medicinal chemistry. The boronic acid moiety allows for interactions with biological targets, making it useful in drug development, particularly in the context of cancer therapy and other diseases where targeting specific biomolecules is crucial. Additionally, the compound's structure suggests potential for use in cross-coupling reactions, a key process in organic synthesis. Its solubility and stability in various solvents can vary, influencing its reactivity and application in different chemical environments. Overall, B-[3-[(Methylphenylamino)methyl]phenyl]boronic acid exemplifies the versatility of boronic acids in both synthetic and biological chemistry.

Formula: C₁₄H₁₆BNO₂

InChI: InChI=1S/C14H16BNO2/c1-16(14-8-3-2-4-9-14)11-12-6-5-7-13(10-12)15(17)18/h2-10,17-18H,11H2,1H3

InChI key: InChIKey=ZJQLMGRDWCNSQU-UHFFFAOYSA-N

SMILES: C(N(C)C1=CC=CC=C1)C2=CC(B(O)O)=CC=C2

Synonyms:

• Boronic acid, B-[3-[(methylphenylamino)methyl]phenyl]-
• B-[3-[(Methylphenylamino)methyl]phenyl]boronic acid

(3-((methyl(phenyl)amino)methyl)phenyl)boronic acid

CAS: 1334226-27-5

Formula: C₁₄H₁₆BNO₂

Purity: 95%

Color and Shape: Solid

Molecular weight: 241.0933

Ref: IN-DA01FNMK