CAS 3848-36-0
:1-(4-chlorophenyl)-N-hydroxymethanimine
Description:
1-(4-chlorophenyl)-N-hydroxymethanimine, with the CAS number 3848-36-0, is an organic compound characterized by its unique functional groups. It features a hydroxymethanimine moiety, which is a derivative of methanimine where one of the hydrogen atoms is replaced by a hydroxyl group. The presence of the 4-chlorophenyl group indicates that the compound has a chlorinated aromatic ring, which can influence its reactivity and physical properties. This 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 organic synthesis and medicinal chemistry, particularly in the development of pharmaceuticals or agrochemicals. The chlorophenyl substituent may enhance biological activity or alter the compound's interaction with biological targets. As with many organic compounds, safety precautions should be taken when handling it, as it may pose health risks or environmental hazards.
Formula:C7H6ClNO
InChI:InChI=1/C7H6ClNO/c8-7-3-1-6(2-4-7)5-9-10/h1-5,10H
SMILES:c1cc(ccc1C=NO)Cl
Synonyms:- 3848-36-0
- Benzaldoxime, 4-chloro-
- Qnu1R Dg
- 1-(4-Chlorophenyl)-N-hydroxymethanimine
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Found 4 products.
4-Chlorobenzenecarbaldehyde oxime
CAS:Formula:C7H6ClNOPurity:98%Color and Shape:SolidMolecular weight:155.58164-Chlorobenzaldoxime
CAS:4-ChlorobenzaldoximePurity:≥95%Color and Shape:SolidMolecular weight:155.58g/mol4-Chlorobenzaldehyde oxime
CAS:<p>4-Chlorobenzaldehyde oxime is an antibacterial agent that is classified as a chloroamine. It has been shown to be an effective inhibitor of bacterial growth, with a low toxicity to mammalian cells. 4-Chlorobenzaldehyde oxime has been shown to be activated by amines and hydroxylamine, and the resulting intermediate can cleave a variety of bonds in the bacterial cell wall. The molecular orbitals of this compound have been calculated using crystallographic data and functional theory. 4-Chlorobenzaldehyde oxime also binds to chloride ions and forms a complex with ammonium nitrate, which may account for its activity against some bacteria that are resistant to chlorinated compounds (e.g., Clostridium difficile). This compound also contains functional groups that may react with disulfides present in the bacterial cell wall.</p>Formula:C7H6ClNOPurity:Min. 95%Color and Shape:PowderMolecular weight:155.58 g/mol4-Chlorobenzenecarbaldehyde oxime
CAS:Formula:C7H6ClNOPurity:98%Color and Shape:SolidMolecular weight:155.58



