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CAS 88978-20-5

:

[3-[(2,2,2-trifluoroacetyl)amino]phenyl]boronic acid

Description:
[3-[(2,2,2-trifluoroacetyl)amino]phenyl]boronic acid, with the CAS number 88978-20-5, is a boronic acid derivative characterized by the presence of a boron atom bonded to a phenyl group and an amino group that is further substituted with a trifluoroacetyl 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 trifluoroacetyl group enhances its lipophilicity and may influence its biological activity. Additionally, the presence of the boronic acid functional group allows for potential interactions with biological targets, which can be exploited in drug design. The compound is likely to be solid at room temperature and may exhibit moderate solubility in polar solvents. Its reactivity and stability can be influenced by environmental factors such as pH and temperature, which are important considerations in its handling and application in research.
Formula:C8H7BF3NO3
InChI:InChI=1/C8H7BF3NO3/c10-8(11,12)7(14)13-6-3-1-2-5(4-6)9(15)16/h1-4,15-16H,(H,13,14)
SMILES:c1cc(cc(c1)N=C(C(F)(F)F)O)B(O)O
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