CAS 611-35-8
:4-Chloroquinoline
Description:
4-Chloroquinoline is a heterocyclic organic compound characterized by a quinoline structure with a chlorine substituent at the fourth position. It has a molecular formula of C9H6ClN and features a bicyclic system composed of a benzene ring fused to a pyridine ring. This compound typically appears as a yellowish to brown solid and is known for its aromatic properties, which contribute to its stability and reactivity. 4-Chloroquinoline is soluble in organic solvents such as ethanol and ether but has limited solubility in water. It is primarily used in the synthesis of pharmaceuticals, agrochemicals, and as an intermediate in organic synthesis. Additionally, it exhibits biological activity, making it of interest in medicinal chemistry, particularly in the development of antimalarial and antimicrobial agents. Safety considerations include handling it with care due to its potential toxicity and environmental impact. Proper storage and disposal methods should be followed to mitigate any risks associated with its use.
Formula:C9H6ClN
InChI:InChI=1S/C9H6ClN/c10-8-5-6-11-9-4-2-1-3-7(8)9/h1-6H
InChI key:InChIKey=KNDOFJFSHZCKGT-UHFFFAOYSA-N
SMILES:ClC=1C2=C(N=CC1)C=CC=C2
Synonyms:- N-Chloroquinoline
- NSC 96902
- Quinoline, 4-chloro-
- 4-Chloroquinoline
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Found 7 products.
4-Chloroquinoline
CAS:Formula:C9H6ClNPurity:>97.0%(GC)Color and Shape:White to Almost white powder to lumpMolecular weight:163.604-Chloroquinoline, 99%
CAS:<p>It is an important raw material and intermediate used in organic synthesis, pharmaceuticals, agrochemicals and dyestuffs. This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. Th</p>Formula:C9H6ClNPurity:99%Molecular weight:163.604-Chloroquinoline
CAS:4-ChloroquinolineFormula:C9H6ClNPurity:98%Color and Shape: pale yellow powderMolecular weight:163.60g/mol4-Chloroquinoline
CAS:4-Chloroquinoline is a quinoline derivative that has been used in the synthesis of other organic compounds. It is used to form alkylating agents, which are reactive and can react with double or triple bonds in organic molecules. 4-Chloroquinoline may be used as a nucleophile and is also capable of forming covalent bonds with electron-rich groups such as chloride ions. It can also undergo reactions with electrophiles, such as halides or carboxylic acids, to form carbonium ions. 4-Chloroquinoline is an alkylation agent, which is a chemical compound that reacts with an unsaturated compound by adding one or more alkyl groups. The most common reaction of 4-chloroquinoline is the Suzuki coupling reaction, which involves the addition of two equivalents of boronic acid to the quinoline molecule. This reaction creates an n-oxide group on the quinoline ring and formsFormula:C9H6ClNPurity:Min. 95%Molecular weight:163.6 g/mol






