CAS 57334-36-8
:4-Chloro-8-hydroxyquinoline
Description:
4-Chloro-8-hydroxyquinoline is an organic compound characterized by its quinoline structure, which features a chlorine atom at the 4-position and a hydroxyl group at the 8-position. This compound is typically a pale yellow to brown solid and is known for its potential applications in various fields, including pharmaceuticals and biochemistry. It exhibits properties such as being a weakly acidic compound due to the presence of the hydroxyl group, which can participate in hydrogen bonding. The chlorine substituent can influence its reactivity and solubility in organic solvents. Additionally, 4-Chloro-8-hydroxyquinoline has been studied for its antimicrobial and antifungal activities, making it of interest in medicinal chemistry. Its molecular structure allows for interactions with biological targets, which can be leveraged in drug development. Safety data indicates that, like many chemical substances, it should be handled with care, as it may pose health risks if ingested or inhaled. Overall, this compound's unique characteristics make it a subject of interest in both research and industrial applications.
Formula:C9H6ClNO
InChI:InChI=1S/C9H6ClNO/c10-7-4-5-11-9-6(7)2-1-3-8(9)12/h1-5,12H
InChI key:InChIKey=DEPRJVQVGXOXRN-UHFFFAOYSA-N
SMILES:ClC=1C2=C(C(O)=CC=C2)N=CC1
Synonyms:- 4-Chloro-8-quinolinol
- 4-Chloroquinolin-8-ol
- 8-Quinolinol, 4-Chloro-
- NSC 673455
- 4-Chloro-8-hydroxyquinoline
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Found 6 products.
4-CHLORO-8-HYDROXYQUINOLINE
CAS:Formula:C9H6ClNOPurity:98%Color and Shape:SolidMolecular weight:179.60304-Chloroquinolin-8-ol
CAS:<p>4-Chloroquinolin-8-ol is a building block</p>Formula:C9H6ClNOPurity:98.8%Color and Shape:SolidMolecular weight:179.64-Chloro-8-quinolinol
CAS:<p>4-Chloro-8-quinolinol is a quinoline derivative that has been shown to have pharmacological effects. It is used in the synthesis of other compounds, such as 5-chloro-8-hydroxyquinoline, which is used in the treatment of cancer. 4-Chloro-8-quinolinol can also be prepared by oxidizing 5,6,7,8 tetrachloroquinoline with chlorine and ammonia. The photophysical properties of this compound are analogous to those of benzothiazole derivatives. The fluorescence emission spectrum ranges from 360 nm to 450 nm with a maximum at 390 nm and emission intensity at 350 nm. This compound exhibits fungitoxicity against Penicillium notatum and Aspergillus fumigatus.</p>Formula:C9H6ClNOPurity:Min. 95%Molecular weight:179.6 g/mol




