4,7-Dichloroquinoline, 98%
4,7-Dichloroquinoline, 98%
4,7-Dichloroquinoline, 98%
Thermo Scientific Chemicals

4,7-Dichloroquinoline, 98%

CAS: 86-98-6 | C9H5Cl2N | 198.046 g/mol
Quantity:
25 g
100 g
Catalog number A15985.14
also known as A15985-14
Price (JPY)
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Quantity:
25 g
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Chemical Identifiers
CAS86-98-6
IUPAC Name4,7-dichloroquinoline
Molecular FormulaC9H5Cl2N
InChI KeyHXEWMTXDBOQQKO-UHFFFAOYSA-N
SMILESClC1=CC=C2C(Cl)=CC=NC2=C1
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SpecificationsSpecification SheetSpecification Sheet
FormCrystals or powder or crystalline powder
Assay (GC)≥97.5%
Identification (FTIR)Conforms
Melting Point (clear melt)82.0-88.0?C
Appearance (Color)White to cream to yellow to pale brown
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.

Suitable for battery materials development.

Applications
4,7-Dichloroquinoline is used as a drug chloroquine phosphate intermediate. It is also is used in the synthesis of hybrid aminoquinoline-triazine derivatives that show anti-microbial activity. In addition, it is used in the synthesis of novel oxazolidinones as anti-microbial agents showing efficacy against common bacterial strains.

Solubility
Insoluble in water.

Notes
Keep container tightly sealed. Store in cool, dry conditions in well sealed containers. Incompatible with oxidizing agents.
RUO – Research Use Only

General References:

  1. Alexander R. Surrey.; Royal A. Cutler. The Role of Phenol in the Reaction of 4,7-Dichloroquinoline with Novol Diamine. J. Am. Chem. Soc. 1951, 73 (6), 2623-2626.
  2. Robert C. Elderfield.; Walter J. Gensler.; Oskar Birstein.; Frank J. Kreysa.; John T. Maynard.; Jean Galbreath. Synthesis of Certain Simple 4-Aminoquinoline Derivatives. J. Am. Chem. Soc. 1946, 68 (7), 1250-1251.