CAS 1334399-67-5
:B-[2-Fluoro-5-(4-morpholinylmethyl)phenyl]boronic acid
Description:
B-[2-Fluoro-5-(4-morpholinylmethyl)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 and is widely used in organic synthesis and medicinal chemistry. The compound features a fluorinated phenyl ring, which can enhance its biological activity and lipophilicity. The morpholinylmethyl substituent contributes to its solubility and potential interactions with biological targets, making it of interest in drug development. This compound may exhibit properties such as moderate to high stability under standard conditions, and its boronic acid moiety can participate in Suzuki coupling reactions, facilitating the formation of carbon-carbon bonds. Additionally, the presence of the fluorine atom may influence the electronic properties of the molecule, potentially affecting its reactivity and interaction with biological systems. Overall, B-[2-Fluoro-5-(4-morpholinylmethyl)phenyl]boronic acid represents a versatile structure in the realm of synthetic and medicinal chemistry.
Formula:C11H15BFNO3
InChI:InChI=1S/C11H15BFNO3/c13-11-2-1-9(7-10(11)12(15)16)8-14-3-5-17-6-4-14/h1-2,7,15-16H,3-6,8H2
InChI key:InChIKey=IAANUHQAUPDWNK-UHFFFAOYSA-N
SMILES:C(C1=CC(B(O)O)=C(F)C=C1)N2CCOCC2
Synonyms:- [2-Fluoro-5-(morpholin-4-ylmethyl)phenyl]boronic acid
- Boronic acid, B-[2-fluoro-5-(4-morpholinylmethyl)phenyl]-
- [2-Fluoro-5-[(morpholin-4-yl)methyl]phenyl]boronic acid
- B-[2-Fluoro-5-(4-morpholinylmethyl)phenyl]boronic acid
- (2-Fluoro-5-(morpholinomethyl)phenyl)boronic acid
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Boronic acid, B-[2-fluoro-5-(4-morpholinylmethyl)phenyl]-
CAS:Formula:C11H15BFNO3Color and Shape:SolidMolecular weight:239.0511
