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About This Item
Empirical Formula (Hill Notation):
C9H5Cl2N
CAS Number:
Molecular Weight:
198.05
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
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Assay
97%
form
solid
mp
161-164 °C (lit.)
SMILES string
Clc1ccc2nc(Cl)ccc2c1
InChI
1S/C9H5Cl2N/c10-7-2-3-8-6(5-7)1-4-9(11)12-8/h1-5H
InChI key
LPDFGLZUUCLXGM-UHFFFAOYSA-N
General description
2,6-Dichloroquinoline can be synthesized from 6-chloroquinoline. It can also be prepared from the corresponding 2-vinylaniline.
Application
2,6-Dichloroquinoline may be used in the preparation of poly(quinoline-2,6-diyl), via electrochemical polymerization.
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
Target Organs
Respiratory system
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Certificates of Analysis (COA)
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Electrochemical and chemical preparation of linear. pi.-conjugated poly (quinoline-2, 6-diyl) using nickel complexes and electrochemical properties of the polymer.
Saito N, et al.
Macromolecules, 27(3), 756- 761 (1994)
Poly (1, 5-naphthyridine-2, 6-diyl) Having a Highly Extended and Electron-Withdrawing. pi.-Conjugation System. Preparation, Optical Properties, and Electrochemical Redox Reaction.
Saito N and Yamamoto T.
Macromolecules, 28(12), 4260-4267 (1995)
Byoung Se Lee et al.
The Journal of organic chemistry, 67(22), 7884-7886 (2002-10-26)
2-Vinyl- or heteroaryl-substituted anilines were reacted with diphosgene in acetonitrile solution via a reactive imidoyl moiety to afford the corresponding 2-chloroquinolines. Facile syntheses of nine 2-chloroquinoline derivatives from several anilines and their postulate mechanism is described. The postulate mechanism of
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