Quinoline, 6,7-dimethoxy-4-(4-nitrophenoxy)-

CAS NO.： 190728-24-6

Purity: 98%
Appearance: Yellow to orange yellow crystalline powder

Product name	Quinoline, 6,7-dimethoxy-4-(4-nitrophenoxy)-
Synonym	Quinoline,6,7-dimethoxy-4-(4-nitrophenoxy)-;6,7-dimethoxy-4-(4-nitrophenoxy)-Quinoline;CabozantinibGenotoxicImpurityII;6,7-dimethoxy-4-(4-nitrophenoxy)quinolineQ:Whatis6,7-dimethoxChemicalbooky-4-(4-nitrophenoxy)quinolineQ:WhatistheCASNumberof6,7-dimethoxy-4-(4-nitrophenoxy)quinoline;CabozantinibNitroAnalog;6,7-dimethoxy-4-(4-nitrophenoxy)quinoline?(CabozantinibImpurity）
CAS NO.	190728-24-6
Appearance	Yellow to orange yellow crystalline powder
Purity	98%
MF	C17H14N2O5
MW	326.3
Related categories	Impurity reference substance – Cabozantinib
Structural formula
Product Manager Email:	ada@coreychem.com

Pharmaceuticals and bioactive molecules
1. Research on anti malaria: Derivatives of quinoline compounds (such as chloroquine) may serve as intermediates or analogues for anti malaria drugs.
2. Antitumor potential: Quinoline skeleton can be embedded in DNA, and nitrophenyl may enhance cytotoxicity (further activity testing is needed).
3. Kinase inhibitor: a synthetic precursor of protein kinase (such as EGFR, CDK) inhibitors.
Organic optoelectronic materials
1. Fluorescent probe: can be used for biological imaging or metal ion detection (nitrophenyl may participate in coordination).
2. OLED materials: Quinoline derivatives are commonly used in electron transport layers (ETL) or emissive layers (EML).
Chemical synthesis intermediates
1. Nitro reduction: can be converted into aminophenylquinoline for further modification (such as coupling reaction).
2. Suzuki coupling: Reacting with boronic acid derivatives to construct more complex conjugated systems.

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