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
製品番号(カタログ番号) H54895.03
または、製品番号H54895-03
価格(JPY)
-
数量:
1 g
一括またはカスタム形式をリクエストする
化学物質識別子
CAS1810-71-5
IUPAC Name6-bromo-2-chloroquinoline
Molecular FormulaC9H5BrClN
InChI KeyYXRDWUJAJLDABJ-UHFFFAOYSA-N
SMILESClC1=NC2=CC=C(Br)C=C2C=C1
さらに表示
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.