CAS 15644-86-7
:6-Chloro-4-hydroxy-2-methylquinoline
Description:
6-Chloro-4-hydroxy-2-methylquinoline, with the CAS number 15644-86-7, is a heterocyclic organic compound belonging to the quinoline family. It features a chlorine atom at the 6-position and a hydroxyl group at the 4-position of the quinoline ring, along with a methyl group at the 2-position. This compound is characterized by its aromatic structure, which contributes to its stability and reactivity. The presence of the hydroxyl group imparts polar characteristics, enhancing its solubility in polar solvents. Additionally, the chlorine substituent can influence its reactivity, making it a potential candidate for various chemical reactions, including nucleophilic substitutions. 6-Chloro-4-hydroxy-2-methylquinoline may exhibit biological activity, which has led to interest in its potential applications in pharmaceuticals and agrochemicals. Its unique structural features allow for further exploration in medicinal chemistry, particularly in the development of compounds with antimicrobial or anti-inflammatory properties. Overall, this compound represents a significant interest in both synthetic and applied chemistry fields.
Formula:C10H8ClNO
InChI:InChI=1/C10H8ClNO/c1-6-4-10(13)8-5-7(11)2-3-9(8)12-6/h2-5H,1H3,(H,12,13)
InChI key:InChIKey=VGDMRXDQWBBKBW-UHFFFAOYSA-N
SMILES:OC=1C2=C(N=C(C)C1)C=CC(Cl)=C2
Synonyms:- 4-Quinolinol, 6-chloro-2-methyl-
- 6-Chloro-2-Methylquinolin-4-Ol
- 6-Chloro-2-methyl-4-quinolinol
- 6-chloro-2-methylquinolin-4(1H)-one
- 6-Chloro-4-hydroxy-2-methylquinoline
- 6-CHLORO-4-HYDROXYQUINALDINE
- 2-Methyl-4-hydroxy-6-chloroquinoline
- AURORA 18121
- 6-CHLORO-2-METHYL-4(1H)QUINOLONE
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Found 4 products.
6-Chloro-2-methylquinolin-4-ol
CAS:Formula:C10H8ClNOPurity:97%Color and Shape:SolidMolecular weight:193.62966-Chloro-4-hydroxy-2-methylquinoline
CAS:<p>6-Chloro-4-hydroxy-2-methylquinoline</p>Purity:98%Molecular weight:193.63g/mol6-Chloro-4-hydroxy-2-methylquinoline
CAS:<p>6-Chloro-4-hydroxy-2-methylquinoline is a vasorelaxant that blocks potassium channels in the cell membrane. 6CHMQ has been shown to inhibit calcium and potassium channels, which are involved in the transmission of nerve impulses. It also inhibits glibenclamide binding to pancreatic beta cells, which is an action that contributes to the anti-diabetic effects of this drug. 6CHMQ has been shown to block voltage gated potassium channels and may have a role in regulating blood pressure by inhibiting the release of norepinephrine.</p>Formula:C10H8ClNOPurity:Min. 95%Molecular weight:193.63 g/mol



