CAS 171922-46-6
:4-(N-Propylaminocarbonyl)phenylboronic acid
Description:
4-(N-Propylaminocarbonyl)phenylboronic acid is an organic compound characterized by the presence of a boronic acid functional group attached to a phenyl ring, which is further substituted with a propylaminocarbonyl group. This compound typically exhibits properties associated with both boronic acids and amides, including the ability to form reversible covalent bonds with diols, making it useful in various applications such as drug development and materials science. The boronic acid moiety allows for potential interactions with biological molecules, which can be exploited in medicinal chemistry for targeted drug delivery or as a tool in biochemical assays. Additionally, the presence of the propylaminocarbonyl group may influence its solubility and reactivity, enhancing its utility in synthetic pathways. The compound is likely to be a solid at room temperature and may exhibit moderate stability under standard conditions, although it is sensitive to moisture due to the boronic acid functionality. Overall, its unique structural features make it a valuable compound in both research and industrial applications.
Formula:C10H14BNO3
InChI:InChI=1/C10H14BNO3/c1-2-7-12-10(13)8-3-5-9(6-4-8)11(14)15/h3-6,14-15H,2,7H2,1H3,(H,12,13)
SMILES:CCCNC(=O)c1ccc(cc1)B(O)O
Synonyms:- [4-(Propylcarbamoyl)Phenyl]Boronic Acid
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Found 3 products.
4-(N-Propylaminocarbonyl)phenylboronic acid
CAS:Formula:C10H14BNO3Purity:98%Color and Shape:SolidMolecular weight:207.03414-(Propylcarbamoyl)benzeneboronic acid
CAS:4-(Propylcarbamoyl)benzeneboronic acidPurity:≥95%Color and Shape:White SolidMolecular weight:207.03g/mol


