2-Chloro-6-methoxyquinoline-3-carboxaldehyde, 99%
2-Chloro-6-methoxyquinoline-3-carboxaldehyde, 99%
2-Chloro-6-methoxyquinoline-3-carboxaldehyde, 99%
Thermo Scientific Chemicals

2-Chloro-6-methoxyquinoline-3-carboxaldehyde, 99%

CAS: 73568-29-3 | C11H8ClNO2 | 221.64 g/mol
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5 g
25 g
Catalog number H26973.06
also known as H26973-06
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5 g
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Chemical Identifiers
CAS73568-29-3
IUPAC Name2-chloro-6-methoxyquinoline-3-carbaldehyde
Molecular FormulaC11H8ClNO2
InChI KeyTZQOMBXDCIPJKW-UHFFFAOYSA-N
SMILESCOC1=CC=C2N=C(Cl)C(C=O)=CC2=C1
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SpecificationsSpecification SheetSpecification Sheet
Appearance (Color)Yellow to pale orange or pale brown
Assay (GC)≥98.5%
Free acid (titration)≤0.5%
Melting Point (clear melt)145-151?C
FormPowder
Mainly used as solvents. They are used in intermediate steps for the production of paints, plastics, synthetic resins, and dyes. They are also used in the manufacture of perfumes, solvents, and flavorings. As raw material in organic synthesis.

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. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

Applications
Mainly used as solvents. They are used in intermediate steps for the production of paints, plastics, synthetic resins, and dyes. They are also used in the manufacture of perfumes, solvents, and flavorings. As raw material in organic synthesis.

Solubility
Insoluble in water.

Notes
Air Sensitive. Store in cool place. Keep container tightly closed in a dry and well-ventilated place. Store away from strong oxidizing agents, air.
RUO – Research Use Only

General References:

  1. Subashini,; S. Mohana Roopan,; F. nawaz khan. Synthesis and Free Radical Scavenging Property of some Quinoline Derivatives. J. Chil. Chem. Soc. 2010, 55 (3),317-319.
  2. F. N. Khan,; R. Subashini,; S. M. Roopan,; V. R. Hathwar,;S. W. Ng. 2-Chloro-6-methyl­quinoline-3-carbaldehyde . Journal name. year of publication , volume issue , pg no.