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CAS 850589-40-1

:

B-[3-Chloro-4-[(ethylamino)carbonyl]phenyl]boronic acid

Description:
B-[3-Chloro-4-[(ethylamino)carbonyl]phenyl]boronic acid, with the CAS number 850589-40-1, is a boronic acid derivative characterized by its boron atom bonded to a phenyl ring that contains a chloro substituent and an ethylamino carbonyl 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 presence of the chloro group can influence its reactivity and solubility, while the ethylamino carbonyl moiety may enhance its biological activity or interaction with specific targets. Boronic acids are often employed in the development of pharmaceuticals, particularly in the context of protease inhibitors and other therapeutic agents. Additionally, this compound may exhibit moderate to high polarity due to the functional groups present, affecting its solubility in different solvents. Overall, B-[3-Chloro-4-[(ethylamino)carbonyl]phenyl]boronic acid is a versatile compound with potential applications in chemical research and drug development.
Formula:C9H11BClNO3
InChI:InChI=1S/C9H11BClNO3/c1-2-12-9(13)7-4-3-6(10(14)15)5-8(7)11/h3-5,14-15H,2H2,1H3,(H,12,13)
InChI key:InChIKey=HJDYETAQUCUPFP-UHFFFAOYSA-N
SMILES:C(NCC)(=O)C1=C(Cl)C=C(B(O)O)C=C1
Synonyms:
  • B-[3-Chloro-4-[(ethylamino)carbonyl]phenyl]boronic acid
  • Boronic acid, [3-chloro-4-[(ethylamino)carbonyl]phenyl]-
  • [3-Chloro-4-(ethylcarbamoylcarbonyl)phenyl]boronic acid
  • boronic acid, B-[3-chloro-4-[(ethylamino)carbonyl]phenyl]-
  • [3-Chloro-4-(ethylcarbamoyl)phenyl]boronic acid
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