CAS 90084-66-5
:[3-(carbamoylamino)phenyl]boronic acid
Description:
[3-(Carbamoylamino)phenyl]boronic acid, with the CAS number 90084-66-5, is an organic compound that features a boronic acid functional group attached to a phenyl ring substituted with a carbamoylamino group. This compound typically exhibits characteristics common to 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 carbamoylamino group enhances its solubility in polar solvents and may influence its reactivity and biological activity. Additionally, boronic acids are known for their role in Suzuki coupling reactions, which are essential in the formation of carbon-carbon bonds. The compound's structure suggests potential applications in drug development, particularly in targeting specific biological pathways or as a building block in the synthesis of more complex molecules. Overall, [3-(carbamoylamino)phenyl]boronic acid is a versatile compound with significant implications in both synthetic and medicinal chemistry.
Formula:C7H9BN2O3
InChI:InChI=1/C7H9BN2O3/c9-7(11)10-6-3-1-2-5(4-6)8(12)13/h1-4,12-13H,(H3,9,10,11)
SMILES:c1cc(cc(c1)NC(=N)O)B(O)O
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Found 3 products.
[3-(Carbamoylamino)phenyl]boronic acid
CAS:<p>Versatile small molecule scaffold</p>Formula:C7H9BN2O3Purity:Min. 95%Molecular weight:179.97 g/mol


