CAS 23964-29-6
:3,5-dichloro-4-hydroxybenzohydrazide
Description:
3,5-Dichloro-4-hydroxybenzohydrazide is an organic compound characterized by its hydrazide functional group and the presence of chlorine and hydroxyl substituents on a benzene ring. It features two chlorine atoms located at the 3 and 5 positions and a hydroxyl group at the 4 position of the aromatic ring, contributing to its chemical reactivity and potential biological activity. The compound is typically a solid at room temperature and may exhibit moderate solubility in polar solvents due to the hydroxyl group. Its structure suggests potential applications in pharmaceuticals, agrochemicals, or as a reagent in organic synthesis. The presence of halogen atoms often enhances the compound's reactivity, making it useful in various chemical reactions. Additionally, the hydrazide moiety can participate in condensation reactions, further expanding its utility in synthetic chemistry. Safety data should be consulted for handling, as halogenated compounds can pose health risks. Overall, 3,5-dichloro-4-hydroxybenzohydrazide is a compound of interest in both research and industrial applications.
Formula:C7H6Cl2N2O2
InChI:InChI=1/C7H6Cl2N2O2/c8-4-1-3(7(13)11-10)2-5(9)6(4)12/h1-2,12H,10H2,(H,11,13)
SMILES:c1c(cc(c(c1Cl)O)Cl)C(=NN)O
Synonyms:- Benzoic Acid, 3,5-Dichloro-4-Hydroxy-, Hydrazide
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