6-Bromo-2-chloroquinoline, 96%
6-Bromo-2-chloroquinoline, 96%
6-Bromo-2-chloroquinoline, 96%
Thermo Scientific Chemicals

6-Bromo-2-chloroquinoline, 96%

CAS: 1810-71-5 | C9H5BrClN | 242.50 g/mol
Quantity:
1 g
5 g
Catalog number H54895.03
also known as H54895-03
Price (JPY)
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Quantity:
1 g
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Chemical Identifiers
CAS1810-71-5
IUPAC Name6-bromo-2-chloroquinoline
Molecular FormulaC9H5BrClN
InChI KeyYXRDWUJAJLDABJ-UHFFFAOYSA-N
SMILESClC1=NC2=CC=C(Br)C=C2C=C1
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SpecificationsSpecification SheetSpecification Sheet
Appearance (Color)White to off-white
Proton NMRConforms
Purity≥95.0%
FormSolid
It is used as a pharmaceutical intermediate.

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 used as a pharmaceutical intermediate.

Solubility
Soluble in Chloroform and Methanol

Notes
Store at room temperature with proper ventilation.
RUO – Research Use Only

General References:

  1. Jessica A. Smith.; Rhiannon K. Jones.; Grant W. Booker.; Simon M. Pyke. Sequential and Selective Buchwald-Hartwig Amination Reactions for the Controlled Functionalization of 6-Bromo-2-chloroquinoline: Synthesis of Ligands for the Tec Src Homology 3 Domain. J. Org. Chem. 2008, 73 (22),8880-8892.
  2. Eckhard Baston.; Anja Palusczak.; Rolf W. Hartmann. 6-Substituted 1H-quinolin-2-ones and 2-methoxy-quinolines: Synthesis and evaluation as inhibitors of steroid 5α reductases types 1 and 2. Eur. J. Med. Chem. 2000, 35 (10),931-940.