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CAS 850589-37-6

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[3-chloro-4-(hydrazinecarbonyl)phenyl]boronic acid

Description:
[3-chloro-4-(hydrazinecarbonyl)phenyl]boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group, which is known for its ability to form reversible covalent bonds with diols. This compound features a phenyl ring substituted with a chlorine atom and a hydrazinecarbonyl group, which contributes to its reactivity and potential applications in medicinal chemistry and organic synthesis. The hydrazinecarbonyl moiety can participate in various chemical reactions, including coupling reactions and the formation of hydrazones. The boronic acid group allows for participation in Suzuki-Miyaura cross-coupling reactions, making it valuable in the synthesis of complex organic molecules. Additionally, the presence of the chlorine atom may influence the compound's solubility and reactivity. Overall, [3-chloro-4-(hydrazinecarbonyl)phenyl]boronic acid is a versatile compound with potential applications in drug development and materials science, particularly in the synthesis of biologically active compounds and polymers.
Formula:C7H8BClN2O3
InChI:InChI=1/C7H8BClN2O3/c9-6-3-4(8(13)14)1-2-5(6)7(12)11-10/h1-3,13-14H,10H2,(H,11,12)
SMILES:c1cc(c(cc1B(O)O)Cl)C(=NN)O
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