CAS 1287753-40-5
:B-[4-[1-(1-Piperidinyl)ethyl]phenyl]boronic acid
Description:
B-[4-[1-(1-Piperidinyl)ethyl]phenyl]boronic acid, with the CAS number 1287753-40-5, is an organoboron compound characterized by the presence of a boronic acid functional group attached to a phenyl ring. This compound features a piperidine moiety, which contributes to its potential biological activity, particularly in medicinal chemistry. Boronic acids are known for their ability to form reversible covalent bonds with diols, making them useful in various applications, including drug development and as intermediates in organic synthesis. The presence of the piperidinyl group may enhance the compound's solubility and interaction with biological targets, potentially influencing its pharmacokinetic properties. Additionally, boronic acids can act as inhibitors in enzyme-catalyzed reactions, particularly in the context of protease inhibition. Overall, this compound's unique structure suggests potential utility in pharmaceutical applications, particularly in the development of therapeutics targeting specific biological pathways. However, detailed studies would be necessary to fully elucidate its properties and applications.
Formula:C13H20BNO2
InChI:InChI=1S/C13H20BNO2/c1-11(15-9-3-2-4-10-15)12-5-7-13(8-6-12)14(16)17/h5-8,11,16-17H,2-4,9-10H2,1H3
InChI key:InChIKey=AAVZQQFWPJUBCQ-UHFFFAOYSA-N
SMILES:C(C)(C1=CC=C(B(O)O)C=C1)N2CCCCC2
Synonyms:- [4-[1-(Piperidin-1-yl)ethyl]phenyl]boronic acid
- B-[4-[1-(1-Piperidinyl)ethyl]phenyl]boronic acid
- Boronic acid, B-[4-[1-(1-piperidinyl)ethyl]phenyl]-
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Found 2 products.
[4-(1-Piperidin-1-ylethyl)phenyl]boronic acid
CAS:Formula:C13H20BNO2Purity:95.0%Color and Shape:SolidMolecular weight:233.12

