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
3-(4-fluorophenyl)-1-methyl-N-[(1-methyl-4,5,6,7-tetrahydro-1H-indazol-3-yl)methyl]-1H-pyrazole-5-carboxamide
1-((2-Chloropyrimidin-4-yl)methyl)piperidin-3-ol
(E)-N-((1-methyl-4,5,6,7-tetrahydro-1H-indazol-3-yl)methyl)-2-phenylethenesulfonamide
N-((1-methyl-4,5,6,7-tetrahydro-1H-indazol-3-yl)methyl)-1-(m-tolyl)methanesulfonamide
5-chloro-N-((1-methyl-4,5,6,7-tetrahydro-1H-indazol-3-yl)methyl)thiophene-2-sulfonamide
4-methoxy-2-methyl-N-((1-methyl-4,5,6,7-tetrahydro-1H-indazol-3-yl)methyl)benzenesulfonamide
methyl 4-(N-((1-methyl-4,5,6,7-tetrahydro-1H-indazol-3-yl)methyl)sulfamoyl)benzoate
1-ethyl-3-((1-methyl-4,5,6,7-tetrahydro-1H-indazol-3-yl)methyl)urea
1-((1-methyl-4,5,6,7-tetrahydro-1H-indazol-3-yl)methyl)-3-phenylurea
1-(4-ethoxyphenyl)-3-((1-methyl-4,5,6,7-tetrahydro-1H-indazol-3-yl)methyl)urea

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