CymitQuimica logo

CAS 1256355-61-9

:

B-[3-Methyl-5-(phenylmethoxy)phenyl]boronic acid

Description:
B-[3-Methyl-5-(phenylmethoxy)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 phenylmethoxy group, contributing to its hydrophobic characteristics, and a methyl substituent that can influence its reactivity and solubility. The boronic acid moiety is significant in various applications, particularly in organic synthesis and medicinal chemistry, where it serves as a key intermediate in the development of pharmaceuticals and agrochemicals. Additionally, boronic acids are utilized in cross-coupling reactions, such as Suzuki-Miyaura coupling, which is essential for forming carbon-carbon bonds. The presence of the phenyl and methyl groups can enhance the compound's stability and reactivity profile, making it a valuable building block in synthetic chemistry. Overall, B-[3-Methyl-5-(phenylmethoxy)phenyl]boronic acid exemplifies the versatility of boron-containing compounds in modern chemical research and applications.
Formula:C14H15BO3
InChI:InChI=1S/C14H15BO3/c1-11-7-13(15(16)17)9-14(8-11)18-10-12-5-3-2-4-6-12/h2-9,16-17H,10H2,1H3
InChI key:InChIKey=BDGZZCFVEWEVJB-UHFFFAOYSA-N
SMILES:O(CC1=CC=CC=C1)C2=CC(B(O)O)=CC(C)=C2
Synonyms:
  • (3-(Benzyloxy)-5-methylphenyl)boronicacid
  • [3-(Benzyloxy)-5-methylphenyl]boronic acid
  • Boronic acid, B-[3-methyl-5-(phenylmethoxy)phenyl]-
  • B-[3-Methyl-5-(phenylmethoxy)phenyl]boronic acid
  • 3-(Benzyloxy)-5-methylphenylboronic acid
Sort by
Purity (%)
0
100
|
0
|
50
|
90
|
95
|
100
Found 3 products.