[3-(Ethylcarbamoyl)phenyl]boronic acid is an organic compound characterized by the presence of a boronic acid functional group attached to a phenyl ring that is further substituted with an ethylcarbamoyl 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 ethylcarbamoyl moiety contributes to its solubility and reactivity, enhancing its potential as a ligand in coordination chemistry. Additionally, the compound may exhibit biological activity, which can be explored for therapeutic applications. Its structure allows for potential interactions with biological targets, making it of interest in drug development. The compound is usually handled with standard laboratory safety precautions, as with other boronic acids, due to potential reactivity and toxicity. Overall, [3-(ethylcarbamoyl)phenyl]boronic acid represents a versatile building block in chemical synthesis and pharmaceutical research.

[3-(ethylcarbamoyl)phenyl]boronic acid

850567-21-4: boronic acid, B-[3-[(ethylamino)carbonyl]phenyl]-, 3-(N-Ethylaminocarbonyl)phenylboronicacid, 3-(N-Ethylaminocarbonyl)Benzeneboronic Acid, [3-(Ethylcarbamoyl)phenyl]boronic acid

3-(N-Ethylaminocarbonyl)phenylboronic acid

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CAS 850567-21-4: [3-(ethylcarbamoyl)phenyl]boronic acid

3-(N-Ethylaminocarbonyl)phenylboronic acid

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3-(N-Ethylaminocarbonyl)phenylboronic acid

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3-(N-Ethylaminocarbonyl)phenylboronic acid

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3-(Ethylcarbamoyl)benzeneboronic acid

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