86-98-6

  • Product Name:4,7-Dichloroquinoline
  • Structural Formula:C9H5Cl2N
  • Purity:99%
  • Molecular Weight:198.051
Inquiry

Product Details

pd_meltingpoint:81-83 °C(lit.)

Appearance:white to light yellow crystal powder

High Purity 99% supply 4,7-Dichloroquinoline 86-98-6 In Bulk Supply

  • Molecular Formula:C9H5Cl2N
  • Molecular Weight:198.051
  • Appearance/Colour:white to light yellow crystal powder 
  • Vapor Pressure:0.00313mmHg at 25°C 
  • Melting Point:81-83 °C(lit.) 
  • Refractive Index:1.66 
  • Boiling Point:292.9 °C at 760 mmHg 
  • PKA:1.99±0.27(Predicted) 
  • Flash Point:158.7 °C 
  • PSA:12.89000 
  • Density:1.407 g/cm3 
  • LogP:3.54160 

4,7-Dichloroquinoline(Cas 86-98-6) Usage

Chemical Properties

white to light yellow crystal powder

Uses

4,7-Dichloroquinoline is used in the synthesis of hybrid aminoquinoline-triazine derivatives that show anti-microbial activity. In addition, it is used in the synthesis of novel oxazolidinones as anti -microbial agents showing efficacy against common bacterial strains. Chloroquinoline impurity.

General Description

Chloroquine Related Compound A is an impurity of chloroquine, which is a 9-aminoquinoline drug that effectively inhibits viral infections in humans.

Flammability and Explosibility

Notclassified

Purification Methods

Crystallise the dichloroquinoline from MeOH or 95% EtOH. [Beilstein 20/7 V 316.]

InChI:InChI=1/C9H5Cl2N/c10-6-1-2-7-8(11)3-4-12-9(7)5-6/h1-5H

86-98-6 Relevant articles

Highly chemoselective deoxygenation of N-heterocyclic: N -oxides under transition metal-free conditions

Kim, Se Hyun,An, Ju Hyeon,Lee, Jun Hee

supporting information, p. 3735 - 3742 (2021/05/04)

Because their site-selective C-H functio...

Metal-Free Deoxygenation of Amine N-Oxides: Synthetic and Mechanistic Studies

Lecroq, William,Schleinitz, Jules,Billoue, Mallaury,Perfetto, Anna,Gaumont, Annie-Claude,Lalevée, Jacques,Ciofini, Ilaria,Grimaud, Laurence,Lakhdar, Sami

, p. 1237 - 1242 (2021/06/01)

We report herein an unprecedented combin...

Highly Chemoselective Deoxygenation of N-Heterocyclic N-Oxides Using Hantzsch Esters as Mild Reducing Agents

An, Ju Hyeon,Kim, Kyu Dong,Lee, Jun Hee

supporting information, p. 2876 - 2894 (2021/02/01)

Herein, we disclose a highly chemoselect...

Synthesis method of 4,7-dichloroquinoline

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Paragraph 0020; 0027-0028; 0029; 0036-0036; 0038; 0045-0046, (2020/07/15)

The invention discloses a synthesis meth...

86-98-6 Process route

7-chloro-4-hydroxylquinoline
86-99-7

7-chloro-4-hydroxylquinoline

4,7-dichloroquinoline
86-98-6,1138471-54-1

4,7-dichloroquinoline

Conditions
Conditions Yield
With trichlorophosphate; for 1h; Heating;
94%
With trichlorophosphate; Reflux;
89.5%
With trichlorophosphate; for 2h; Heating / reflux;
88.5%
With trichlorophosphate; for 2h; Heating / reflux;
88.5%
With trichlorophosphate; for 6h; Reflux;
81.6%
With trichlorophosphate; for 6h; Reflux;
81.6%
With trichlorophosphate; In toluene; at 100 - 110 ℃; for 5h;
77%
With trichlorophosphate; for 6h; Reflux;
72.7%
With trichlorophosphate;
 
With trichlorophosphate; at 100 ℃;
 
With trichlorophosphate; for 3h; Heating;
 
With trichlorophosphate; at 150 ℃; for 3h;
 
With bis(trichloromethyl) carbonate; N,N-dimethyl-formamide; triphenylphosphine; In toluene; at 50 - 100 ℃; Solvent; Reagent/catalyst;
 
7-chloro-4(1H)-oxoquinoline
23833-97-8

7-chloro-4(1H)-oxoquinoline

4,7-dichloroquinoline
86-98-6,1138471-54-1

4,7-dichloroquinoline

Conditions
Conditions Yield
With trichlorophosphate; for 2h; Reflux;
85%
With trichlorophosphate; for 2h; Reflux;
85%
With ((1,3,5-triazine-2,4,6-triyl)tris(oxy))tris(triphenylphosphonium) chloride; at 140 - 150 ℃; for 2h; Solvent; Ionic liquid;
 
With trichlorophosphate; Reflux;
 

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