CAS 23834-01-7
:4,5,7-Trichloro Quinoline
Description:
4,5,7-Trichloroquinoline is a chemical compound characterized by its quinoline structure, which consists of a fused benzene and pyridine ring. The presence of three chlorine atoms at the 4, 5, and 7 positions of the quinoline ring significantly influences its chemical properties, including its reactivity and solubility. This compound is typically a solid at room temperature and may exhibit a yellowish to brown color. It is known for its potential applications in various fields, including pharmaceuticals and agrochemicals, due to its biological activity. The chlorine substituents can enhance its lipophilicity, affecting its interaction with biological systems. Additionally, 4,5,7-trichloroquinoline may exhibit antimicrobial or antiprotozoal properties, making it of interest in medicinal chemistry. However, handling this compound requires caution due to the toxicity associated with chlorine-containing compounds. Proper safety measures should be observed to mitigate any health risks during its use or study.
Formula:C9H4Cl3N
InChI:InChI=1/C9H4Cl3N/c10-5-3-7(12)9-6(11)1-2-13-8(9)4-5/h1-4H
SMILES:c1cnc2cc(cc(c2c1Cl)Cl)Cl
Synonyms:- Quinoline,4,5,7-Trichloro-
- 4,5,7-Trichloroquinoline
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Found 4 products.
4,5,7-Trichloroquinoline
CAS:4,5,7-TrichloroquinolineFormula:C9H4Cl3NPurity:≥95%Color and Shape: light brown solidMolecular weight:232.49g/mol4,5,7-Trichloroquinoline
CAS:Controlled Product<p>Applications 4,5,7-Trichloroquinoline is an intermediate in synthesizing Quinoxyfen-d4 (Q765502), an isotope labelled Quinoxyfen acts as an agricultural fungicide.<br>References Corrales, M., et al.: Food Chem. Toxicol., 48, 3471 (2010); Lagunas-Allue, L., et al.: Anal. Bioanal. Chem., 398, 1509 (2010); Wong, J., et al.: J. Agric. Food Chem., 58, 5897 (2010);<br></p>Formula:C9H4Cl3NColor and Shape:NeatMolecular weight:232.49




