CymitQuimica logo

CAS 148345-64-6

:

2-ETHOXY-1-NAPHTHALENEBORONIC ACID

Description:
2-Ethoxy-1-naphthaleneboronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a naphthalene ring that is further substituted with an ethoxy group. This compound typically exhibits properties common to boronic acids, such as the ability to form reversible complexes with diols, making it useful in various applications, including organic synthesis and medicinal chemistry. The ethoxy group enhances its solubility in organic solvents, while the naphthalene moiety contributes to its aromatic characteristics, influencing its reactivity and stability. 2-Ethoxy-1-naphthaleneboronic acid can participate in cross-coupling reactions, particularly in the formation of carbon-carbon bonds, which is a valuable process in the synthesis of complex organic molecules. Additionally, its boronic acid functionality allows it to act as a Lewis acid, facilitating various chemical transformations. Overall, this compound is significant in the field of synthetic organic chemistry and has potential applications in drug development and materials science.
Formula:C12H13BO3
InChI:InChI=1/C12H13BO3/c1-2-16-11-8-7-9-5-3-4-6-10(9)12(11)13(14)15/h3-8,14-15H,2H2,1H3
SMILES:CCOc1ccc2ccccc2c1B(O)O
Synonyms:
  • Boronic acid, (2-ethoxy-1-naphthalenyl)- (9CI)
  • (2-Ethoxynaphthalen-1-Yl)Boronic Acid
  • 2-Ethoxy-1-naphthalen-1-ylboronic acid
Sort by
Purity (%)
0
100
|
0
|
50
|
90
|
95
|
100
Found 4 products.