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CAS 850567-31-6

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[3-(2-dimethylaminoethylcarbamoyl)phenyl]boronic acid

Description:
[3-(2-Dimethylaminoethylcarbamoyl)phenyl]boronic acid is an organic compound characterized by the presence of a boronic acid functional group, which is known for its ability to form reversible covalent bonds with diols. This compound features a phenyl ring substituted with a carbamoyl group and a dimethylaminoethyl side chain, contributing to its potential biological activity. The dimethylamino group enhances solubility and may influence the compound's interaction with biological targets. Typically, boronic acids are utilized in medicinal chemistry for their role in drug design, particularly in the development of protease inhibitors and in the synthesis of complex organic molecules through Suzuki coupling reactions. The presence of the boronic acid moiety allows for specific interactions with biomolecules, making it a candidate for applications in targeted therapies. Additionally, the compound's structure suggests potential for modulation of pH-dependent properties, which can be advantageous in various chemical and biological contexts. Overall, [3-(2-dimethylaminoethylcarbamoyl)phenyl]boronic acid represents a versatile scaffold in pharmaceutical research.
Formula:C11H17BN2O3
InChI:InChI=1/C11H17BN2O3/c1-14(2)7-6-13-11(15)9-4-3-5-10(8-9)12(16)17/h3-5,8,16-17H,6-7H2,1-2H3,(H,13,15)
SMILES:CN(C)CCN=C(c1cccc(c1)B(O)O)O
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