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4-Chloroquinoline, 99%, Thermo Scientific Chemicals
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Catalog number H56721.06
also known as H56721-06
Price (USD)/ Each
372.00
-
Quantity:
5 g
Price (USD)/ Each
372.00
4-Chloroquinoline, 99%, Thermo Scientific Chemicals
Catalog numberH56721.06
Price (USD)/ Each
372.00
-
Chemical Identifiers
CAS611-35-8
IUPAC Name4-chloroquinoline
Molecular FormulaC9H6ClN
InChI KeyKNDOFJFSHZCKGT-UHFFFAOYSA-N
SMILESClC1=C2C=CC=CC2=NC=C1
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Specifications
Specification Sheet
Specification SheetAssay (HPLC)>98.5%
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. 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
It is an important raw material and intermediate used in organic synthesis, pharmaceuticals, agrochemicals and dyestuffs.
Solubility
Partly soluble in water.
Notes
Incompatible with oxidizing agents. Store at room temperature.
It is an important raw material and intermediate used in organic synthesis, pharmaceuticals, agrochemicals and dyestuffs.
Solubility
Partly soluble in water.
Notes
Incompatible with oxidizing agents. Store at room temperature.
RUO – Research Use Only
General References:
- O. G. Backeberg. The reaction between phenylhydrazine and 4-chloroquinoline derivatives, and the preparation of the corresponding 4-benzeneazo- and 4-amino-compounds.J. Chem. Soc. 1938, (0),1083-1087.
- Erwan Le Gall.; Corinne Gosmini.; Jean-Yves Nédélec.; Jacques Périchon. Cobalt-catalyzed electrochemical cross-coupling of functionalized phenyl halides with 4-chloroquinoline derivatives. Tetrahedron Lett. 2001 42 (2),267-269.