CymitQuimica logo

CAS 1072952-27-2

:

Boronic acid, B-(2,6-difluoro-3-pyridinyl)-, hydrate (1:1)

Description:
Boronic acid, specifically B-(2,6-difluoro-3-pyridinyl)-, hydrate (1:1), is an organoboron compound characterized by the presence of a boron atom bonded to a pyridine ring that has two fluorine substituents at the 2 and 6 positions. This compound typically exhibits properties associated with boronic acids, such as the ability to form reversible covalent bonds with diols, making it useful in various applications, including organic synthesis and medicinal chemistry. The hydrate form indicates that it contains water molecules in its structure, which can influence its solubility and reactivity. Boronic acids are known for their role in Suzuki coupling reactions, a key method for forming carbon-carbon bonds in organic synthesis. The presence of fluorine atoms can enhance the compound's electronic properties, potentially affecting its reactivity and interaction with biological targets. Overall, this compound's unique structural features and functional properties make it a valuable entity in chemical research and development.
Formula:C5H4BF2NO2·H2O
InChI:InChI=1S/C5H4BF2NO2.H2O/c7-4-2-1-3(6(10)11)5(8)9-4;/h1-2,10-11H;1H2
InChI key:InChIKey=UROAWUNJFURWIY-UHFFFAOYSA-N
SMILES:B(O)(O)C1=C(F)N=C(F)C=C1.O
Synonyms:
  • Boronic acid, B-(2,6-difluoro-3-pyridinyl)-, hydrate (1:1)
Sort by
Purity (%)
0
100
|
0
|
50
|
90
|
95
|
100
Found 2 products.