CAS 850589-51-4
:[3-chloro-4-(pyrrolidine-1-carbonyl)phenyl]boronic acid
Description:
[3-chloro-4-(pyrrolidine-1-carbonyl)phenyl]boronic acid is a boronic acid derivative characterized by the presence of a boron atom bonded to a phenyl ring that is substituted with a chlorine atom and a pyrrolidine-1-carbonyl group. 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 presence of the pyrrolidine moiety may impart specific biological activity or enhance solubility in certain solvents. Additionally, the chlorine substituent can influence the electronic properties of the molecule, potentially affecting its reactivity and interaction with biological targets. The compound is likely to be a solid at room temperature and may have moderate solubility in polar organic solvents. Its unique structure allows for potential applications in drug development, particularly in the design of inhibitors or modulators of biological pathways. As with all chemical substances, proper handling and safety precautions should be observed due to potential toxicity or reactivity.
Formula:C11H13BClNO3
InChI:InChI=1/C11H13BClNO3/c13-10-7-8(12(16)17)3-4-9(10)11(15)14-5-1-2-6-14/h3-4,7,16-17H,1-2,5-6H2
SMILES:C1CCN(C1)C(=O)c1ccc(cc1Cl)B(O)O
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Found 3 products.
(3-Chloro-4-(pyrrolidine-1-carbonyl)phenyl)boronic acid
CAS:Formula:C11H13BClNO3Purity:95%Color and Shape:SolidMolecular weight:253.48983-Chloro-4-(N-pyrrolidin-1-ylcarbonyl)benzeneboronic acid
CAS:3-Chloro-4-(N-pyrrolidin-1-ylcarbonyl)benzeneboronic acidPurity:95%Molecular weight:253.49g/mol(3-Chloro-4-(pyrrolidine-1-carbonyl)phenyl)boronic acid
CAS:Formula:C11H13BClNO3Purity:≥95%Molecular weight:253.49


