• Product Name5-Chloroquinaldine
  • CasNo. 4964-69-6
  • MFC10H8 Cl N
  • MW177.633
  • Purity
  • Appearance
  • Packing
  • Contact usInquiry

Product Details

CasNo: 4964-69-6

MF: C10H8 Cl N

Chinese Manufacturer Supply 5-Chloroquinaldine 4964-69-6 On Stock with Competitive Price

  • Molecular Formula:C10H8 Cl N
  • Molecular Weight:177.633
  • Vapor Pressure:0.007mmHg at 25°C 
  • Melting Point:52-54 ºC 
  • Boiling Point:278.177°C at 760 mmHg 
  • PKA:4.73±0.50(Predicted) 
  • Flash Point:148.736°C 
  • PSA:40.58000 
  • Density:1.225g/cm3 
  • LogP:3.00370 

5-Chloroquinaldine(Cas 4964-69-6) Usage

General Description

5-Chloroquinaldine is an organic chemical compound with the molecular formula C10H8ClN. It is a yellow solid substance that is soluble in organic solvents and exhibits a strong odor. 5-Chloroquinaldine is primarily used as an intermediate in the production of various agrochemicals and pharmaceuticals. It is commonly used as a building block in the synthesis of pesticides, herbicides, and other crop protection products. Additionally, it is utilized in the manufacturing of pharmaceuticals and research chemicals. 5-Chloroquinaldine is considered to be a hazardous substance and should be handled with caution due to its potential health and environmental risks.

InChI:InChI=1/C10H8ClN/c1-7-5-6-8-9(11)3-2-4-10(8)12-7/h2-6H,1H3

4964-69-6 Relevant articles

Quinoline Synthesis by the Reaction of Anilines with 1,2-diols Catalyzed by Iron Compounds

Khusnutdinov, Ravil,Bayguzina, Alfiya,Aminov, Rishat,Dzhemilev, Usein

supporting information, p. 1022 - 1029 (2016/07/28)

The synthesis of quinoline derivatives b...

Quinolines synthesis by reacting 1,3-butanediol with anilines in the presence of iron catalysts

Khusnutdinov,Bayguzina,Aminov

, p. 1613 - 1618 (2016/08/26)

2-, 4-, 6-, 7-, and 8-substituted quinol...

Copper-Promoted Tandem Reaction of Azobenzenes with Allyl Bromides via N=N Bond Cleavage for the Regioselective Synthesis of Quinolines

Yi, Xiangli,Xi, Chanjuan

supporting information, p. 5836 - 5839 (2015/12/11)

A copper-promoted tandem reaction of a v...

Synthesis of substituted quinolines by the reaction of anilines with alcohols and CCl4 in the presence of Fe-containing catalysts

Khusnutdinov,Bayguzina,Aminov

, p. 133 - 137 (2013/11/19)

Substituted quinolines were synthesized ...

4964-69-6 Process route

1.3-butanediol
18826-95-4,107-88-0

1.3-butanediol

3-chloro-aniline
108-42-9

3-chloro-aniline

2-methyl-7-chloroquinoline
4965-33-7

2-methyl-7-chloroquinoline

5-chloro-2-methylquinoline
4964-69-6

5-chloro-2-methylquinoline

7-chloro-4-methyl-quinoline
40941-53-5

7-chloro-4-methyl-quinoline

Conditions
Conditions Yield
With iron(III) chloride hexahydrate; In tetrachloromethane; at 150 ℃; for 8h; Overall yield = 79 %; Inert atmosphere;
(E)-1-Bromo-2-butene
4784-77-4,39616-19-8,29576-14-5

(E)-1-Bromo-2-butene

3,3'-dichloroazobenzene
15426-14-9,106131-20-8,106131-24-2

3,3'-dichloroazobenzene

2-methyl-7-chloroquinoline
4965-33-7

2-methyl-7-chloroquinoline

5-chloro-2-methylquinoline
4964-69-6

5-chloro-2-methylquinoline

Conditions
Conditions Yield
With copper(l) iodide; In 1,2-dichloro-ethane; at 120 ℃; for 12h; Overall yield = 44 %; Overall yield = 15.6 mg; Inert atmosphere; Sealed tube;

4964-69-6 Upstream products

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    75-07-0

    acetaldehyde

  • 108-42-9
    108-42-9

    3-chloro-aniline

  • 106237-28-9
    106237-28-9

    β-(m-chloroanilino)crotonaldehyde

  • 50-00-0
    50-00-0

    formaldehyd

4964-69-6 Downstream products

  • 1027374-02-2
    1027374-02-2

    Acetic acid 3-[(E)-2-(5-chloro-quinolin-2-yl)-vinyl]-phenyl ester

  • 1027848-32-3
    1027848-32-3

    3-[(E)-2-(5-Chloro-quinolin-2-yl)-vinyl]-phenol

  • 108165-12-4
    108165-12-4

    4-{3-[(E)-2-(5-Chloro-quinolin-2-yl)-vinyl]-phenoxy}-butyric acid ethyl ester

  • 143840-93-1
    143840-93-1

    sodium {3-[2-(5-chloro-2-quinolinyl)-(E)-ethenyl]phenoxy}butanoate

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