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(3-Chloro-5-(piperidine-1-carbonyl)phenyl)boronic acid
For research use only. Not for therapeutic Use.
(3-Chloro-5-(piperidine-1-carbonyl)phenyl)boronic acid(CAT: L037080) is a high-purity organoboron compound featuring a chloro-substituted phenyl ring, a boronic acid group, and a piperidine-1-carbonyl moiety. This versatile molecule is widely used in pharmaceutical and organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions for constructing complex molecular frameworks. Its unique structure makes it a valuable intermediate in the development of bioactive compounds, such as enzyme inhibitors and receptor modulators. (3-Chloro-5-(piperidine-1-carbonyl)phenyl)boronic acid supports innovative research in medicinal chemistry, material science, and fine chemical production, offering reliable performance for advanced synthetic applications.
Catalog Number | L037080 |
CAS Number | 957120-47-7 |
Molecular Formula | C12H15BClNO3 |
Purity | ≥95% |
IUPAC Name | [3-chloro-5-(piperidine-1-carbonyl)phenyl]boronic acid |
InChI | InChI=1S/C12H15BClNO3/c14-11-7-9(6-10(8-11)13(17)18)12(16)15-4-2-1-3-5-15/h6-8,17-18H,1-5H2 |
InChIKey | YDTRQMGRXMDOJG-UHFFFAOYSA-N |
SMILES | B(C1=CC(=CC(=C1)Cl)C(=O)N2CCCCC2)(O)O |