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35654-56-9

35654-56-9 Structure

35654-56-9 Structure
IdentificationMore
[Name]

4-CHLORO-6,7-DIMETHOXYQUINOLINE
[CAS]

35654-56-9
[Synonyms]

4-CHLORO-6,7-DIMETHOXYQUINOLINE
6,7-DIMETHOXY-4-CHLOROQUINOLINE
[EINECS(EC#)]

676-028-8
[Molecular Formula]

C11H10ClNO2
[MDL Number]

MFCD07778437
[Molecular Weight]

223.66
[MOL File]

35654-56-9.mol
Chemical PropertiesBack Directory
[Melting point ]

132.0 to 136.0 °C
[Boiling point ]

325.2±37.0 °C(Predicted)
[density ]

1.265±0.06 g/cm3(Predicted)
[storage temp. ]

Keep in dark place,Sealed in dry,Room Temperature
[solubility ]

DMSO (Slightly), Methanol (Slightly)
[form ]

Solid
[pka]

3.95±0.30(Predicted)
[color ]

Pale Brown to Light Brown
[InChI]

InChI=1S/C11H10ClNO2/c1-14-10-5-7-8(12)3-4-13-9(7)6-11(10)15-2/h3-6H,1-2H3
[InChIKey]

WRVHQEYBCDPZEU-UHFFFAOYSA-N
[SMILES]

N1C2C(=CC(OC)=C(OC)C=2)C(Cl)=CC=1
[CAS DataBase Reference]

35654-56-9(CAS DataBase Reference)
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H319-H315-H335
[Precautionary statements ]

P264-P280-P302+P352-P321-P332+P313-P362-P264-P280-P305+P351+P338-P337+P313P
[Hazard Codes ]

T
[Risk Statements ]

25
[Safety Statements ]

45-24/25
[RIDADR ]

UN2811
[WGK Germany ]

WGK 3
[HazardClass ]

IRRITANT
[HS Code ]

29334900
[Storage Class]

6.1C - Combustible acute toxic Cat.3
toxic compounds or compounds which causing chronic effects
[Hazard Classifications]

Acute Tox. 3 Oral
Hazard InformationBack Directory
[Chemical Properties]

Light brown powder
[Uses]

4-Chloro-6,7-dimethoxyquinoline, can be used as an intermediate for the synthesis of various pharmaceutical and biologically active compounds. It is used for the preparation of Tivozanib (T447205), and Cabozantinib (C051500), acting as anticancer agents.
[Application]

4-chloro-6,7-dimethoxy-quinoline can be rich for Buddhist nun with for Wo Zhani medicine as preparing antitumor drug card The key intermediate of thing molecule synthesis.
[Synthesis]

With 3,4-dimethoxyaniline is raw material, obtains aniline compound through nitrification, iron powder reducing, then with Ethyl chloroformate, in Feldalat NM condition cyclization, prepares 4-hydroxyquinoline compounds, after through three Chlorethoxyfos chloro obtains 4-chloro-6,7-dimethoxy-quinoline.
4-chloro-6,7-dimethoxyquinoline synthesis
[References]

[1] Patent: WO2013/180949, 2013, A1. Location in patent: Paragraph 0170
[2] Heterocycles, 2016, vol. 92, # 10, p. 1882 - 1887
[3] Patent: WO2005/121125, 2005, A1. Location in patent: Page/Page column 41-42
[4] Patent: WO2008/48375, 2008, A1. Location in patent: Page/Page column 49
[5] Journal of the American Chemical Society, 1946, vol. 68, p. 1264
Spectrum DetailBack Directory
[Spectrum Detail]

4-CHLORO-6,7-DIMETHOXYQUINOLINE(35654-56-9)1HNMR
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