CAS 2096330-06-0
:B-(3-Amino-2,6-dichlorophenyl)boronic acid
Description:
B-(3-Amino-2,6-dichlorophenyl)boronic acid is a boronic acid derivative characterized by the presence of a boron atom bonded to a phenyl group that is substituted with both amino and dichloro functional groups. 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 amino group can participate in hydrogen bonding and may enhance the compound's solubility in polar solvents. The dichloro substituents can influence the electronic properties of the phenyl ring, potentially affecting reactivity and interaction with biological targets. Additionally, boronic acids are known for their role in the development of pharmaceuticals, particularly in the treatment of diseases like cancer and diabetes, due to their ability to inhibit certain enzymes. Overall, B-(3-Amino-2,6-dichlorophenyl)boronic acid is a versatile compound with significant potential in both research and therapeutic applications.
Formula:C6H6BCl2NO2
InChI:InChI=1S/C6H6BCl2NO2/c8-3-1-2-4(10)6(9)5(3)7(11)12/h1-2,11-12H,10H2
InChI key:InChIKey=HWRKHSZCKZFOMN-UHFFFAOYSA-N
SMILES:B(O)(O)C1=C(Cl)C(N)=CC=C1Cl
Synonyms:- Boronic acid, B-(3-amino-2,6-dichlorophenyl)-
- B-(3-Amino-2,6-dichlorophenyl)boronic acid
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