2,6-Dichloroquinoline

Names

[ Name ]:
2,6-Dichloroquinoline

[Synonym ]:
2,6-Dichlor-chinolin
2,6-Dichloroquinoline
Quinoline, 2,6-dichloro-
MFCD03427194
Quinoline,2,6-dichloro
2-chloro-6-chloroquinoline

Chemical & Physical Properties

[ Density]:
1.4±0.1 g/cm3

[ Boiling Point ]:
292.3±20.0 °C at 760 mmHg

[ Melting Point ]:
161-164ºC

[ Molecular Formula ]:
C₉H₅Cl₂N

[ Molecular Weight ]:
198.049

[ Flash Point ]:
158.4±7.4 °C

[ Exact Mass ]:
196.979904

[ PSA ]:
12.89000

[ LogP ]:
3.27

[ Vapour Pressure ]:
0.0±0.6 mmHg at 25°C

[ Index of Refraction ]:
1.661

[ Storage condition ]:
Room temperature.

MSDS

Safety Information

[ Symbol ]:

GHS07

[ Signal Word ]:
Warning

[ Hazard Statements ]:
H315-H319-H335

[ Precautionary Statements ]:
P261-P305 + P351 + P338

[ Personal Protective Equipment ]:
dust mask type N95 (US);Eyeshields;Gloves

[ Hazard Codes ]:
Xi:Irritant;

[ Risk Phrases ]:
R36/37/38

[ Safety Phrases ]:
S26-S36

[ RIDADR ]:
NONH for all modes of transport

[ WGK Germany ]:
3

[ HS Code ]:
2933499090

Synthetic Route

Click to get detail synthetic route

Customs

[ HS Code ]: 2933499090

[ Summary ]:
2933499090. other compounds containing in the structure a quinoline or isoquinoline ring-system (whether or not hydrogenated), not further fused. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%

Articles

Novel synthesis of 2-chloroquinolines from 2-vinylanilines in nitrile solvent.

J. Org. Chem. 67(22) , 7884-6, (2002)

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...

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)

5-Bromo-2,6-dichloroquinoline
3-benzyl-2,6-dichloroquinoline
2,6-Dichloroquinoline-3-methanol
2,6-Dichloroquinoline-3-carbonitrile
2,6-Dichloroquinoline-3-carbaldehyde
2,6-Dichloroquinoline-4-carbonitrile
N-{bicyclo[1.1.1]pentan-1-yl}-2,2,2-trifluoroacetamide
N-{3-tert-butylbicyclo[1.1.1]pentan-1-yl}-2,2,2-trifluoroacetamide
3-tert-butyl-N-methylbicyclo[1.1.1]pentan-1-amine
1,1-Dimethylethyl N-[3-(1-hydroxy-1-methylethyl)bicyclo[1.1.1]pent-1-yl]carbamate
N-({3-tert-butylbicyclo[1.1.1]pentan-1-yl}methyl)-2,2,2-trifluoroacetamide
tert-Butyl 6-bromo-3-oxo-3H-spiro[isobenzofuran-1,4'-piperidine]-1'-carboxylate
tert-Butyl 2-chloro-5H-spiro[furo[3,4-b]pyridine-7,4'-piperidine]-1'-carboxylate
2-(Pyridin-4-yl)piperidine-2-carbonitrile
1,1-Dioxo-2,3-dihydro-1lambda6-benzothiophene-2-carboxylic acid
5-bromo-6-fluoro-1-(tetrahydro-2H-pyran-2-yl)-1H-indazole

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