
CAS 905971-97-3
:(1-ACETYL-2,3-DIHYDRO-1H-INDOL-5-YL)BORONIC ACID
Description:
(1-Acetyl-2,3-dihydro-1H-indol-5-yl)boronic acid is a boronic acid derivative characterized by its unique structure, which includes an indole moiety and an acetyl group. This compound typically exhibits properties associated with both boronic acids and indole derivatives, such as the ability to form reversible covalent bonds with diols, making it useful in various applications, including organic synthesis and medicinal chemistry. The presence of the boronic acid functional group allows for participation in Suzuki coupling reactions, facilitating the formation of carbon-carbon bonds. Additionally, the indole structure contributes to its potential biological activity, as indoles are known for their roles in pharmaceuticals and natural products. The compound is likely to be a solid at room temperature and may exhibit solubility in polar organic solvents. Its reactivity and functional properties make it a valuable intermediate in the synthesis of more complex organic molecules. Safety and handling precautions should be observed, as with all chemical substances, particularly those containing boron.
Formula:C10H12BNO3
Synonyms:- (1-ACETYL-2,3-DIHYDRO-1H-INDOL-5-YL)BORONIC ACID
- 1-acetylindolin-5-ylboronic acid
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Found 3 products.
(1-acetyl-2,3-dihydro-1H-indol-5-yl)boronic Acid
CAS:Formula:C10H12BNO3Purity:98%Color and Shape:SolidMolecular weight:205.0182(1-Acetylindolin-5-yl)boronic acid
CAS:(1-Acetylindolin-5-yl)boronic acidPurity:98%Molecular weight:205.02g/mol(1-acetyl-2,3-dihydro-1H-indol-5-yl)boronic Acid
CAS:Controlled Product<p>Applications (1-acetyl-2,3-dihydro-1H-indol-5-yl)boronic acid (cas# 905971-97-3) is a useful research chemical.<br></p>Formula:C10H12BNO3Color and Shape:BeigeMolecular weight:205.02


