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CAS 850567-29-2

:

B-[3-[(2-Propen-1-ylamino)carbonyl]phenyl]boronic acid

Description:
B-[3-[(2-Propen-1-ylamino)carbonyl]phenyl]boronic acid, identified by its CAS number 850567-29-2, is a boronic acid derivative characterized by the presence of a boron atom bonded to a phenyl group and an amino acid moiety. 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 propenylamino group suggests potential reactivity and selectivity in biological systems, particularly in targeting specific enzymes or receptors. Additionally, boronic acids are known for their role in drug development, especially in the context of cancer therapeutics and glycoprotein recognition. The compound's solubility, stability, and reactivity can be influenced by its molecular structure, making it a subject of interest in both academic research and industrial applications. Overall, B-[3-[(2-Propen-1-ylamino)carbonyl]phenyl]boronic acid represents a versatile building block in the field of organic and medicinal chemistry.
Formula:C10H12BNO3
InChI:InChI=1S/C10H12BNO3/c1-2-6-12-10(13)8-4-3-5-9(7-8)11(14)15/h2-5,7,14-15H,1,6H2,(H,12,13)
InChI key:InChIKey=BGDGMVTUXWBLLR-UHFFFAOYSA-N
SMILES:C(NCC=C)(=O)C1=CC(B(O)O)=CC=C1
Synonyms:
  • Boronic acid, B-[3-[(2-propen-1-ylamino)carbonyl]phenyl]-
  • B-[3-[(2-Propen-1-ylamino)carbonyl]phenyl]boronic acid
  • (3-(Allylcarbamoyl)phenyl)boronicacid
  • Boronic acid, [3-[(2-propenylamino)carbonyl]phenyl]-
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