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2-Chloroquinoline-4-carbonyl chloride

  • Name 2-Chloroquinoline-4-carbonyl chloride
  • CAS 2388-32-1
  • Purity 99%
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Product Details

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  • Molecular Formula: C10H5Cl2NO
  • Molecular Weight: 226.062
  • Vapor Pressure: 8.17E-05mmHg at 25°C 
  • Melting Point: 89 °C(Solv: benzene (71-43-2)) 
  • Refractive Index: 1.66 
  • Boiling Point: 341.2 °C at 760 mmHg 
  • PKA: -2.82±0.50(Predicted) 
  • Flash Point: 160.2 °C 
  • PSA: 29.96000 
  • Density: 1.457 g/cm3 
  • LogP: 3.26720 

2-Chloroquinoline-4-carbonyl chloride(Cas 2388-32-1) Usage

General Description

2-Chloroquinoline-4-carbonyl chloride is a chemical compound that belongs to the class of organochlorine compounds. These are organic compounds containing a chlorine atom. In particular, this compound contains a quinoline, a nitrogen-containing aromatic compound with a two-ring structure. It is a relatively less researched chemical but is known to be used as a reagent in the synthesis of various complex molecules used in the pharmaceutical and chemical industries. Its properties, such as its physical state, boiling point, melting point, and specific gravity, may vary depending on its purity and other conditional factors. As with many chemicals, it should be handled with care to avoid any harm or reaction.

InChI:InChI=1/C10H5Cl2NO/c11-9-5-7(10(12)14)6-3-1-2-4-8(6)13-9/h1-5H

2388-32-1 Relevant articles

Identification of dibucaine derivatives as novel potent enterovirus 2C helicase inhibitors: In vitro, in vivo, and combination therapy study

Chen, Yinuo,Feng, Leilei,Jin, Mengyu,Lan, Ke,Shu, Ting,Tang, Qi,Wu, Shuwen,Xu, Zhichao,Zhang, Qiuhan,Zhou, Hai-Bing

, (2020)

Enterovirus A71 (EV-A71) is a human path...

Synthesis and antiinflammatory and analgesic activity of 2-substituted cinchoninic acid amides

Pavlova,Mikhalev,Kon'shin,Zaks,Vasilyuk,Vakhrin

, p. 419 - 420 (1999)

-

Method for preparing N-(2-(diethyl)aminoethyl)-2-chloro-4-quinolinecarboxamide

-

Paragraph 0024-0029, (2019/03/08)

The invention discloses a method for pre...

Discovery of Novel Quinoline-Chalcone Derivatives as Potent Antitumor Agents with Microtubule Polymerization Inhibitory Activity

Li, Wenlong,Xu, Feijie,Shuai, Wen,Sun, Honghao,Yao, Hong,Ma, Cong,Xu, Shengtao,Yao, Hequan,Zhu, Zheying,Yang, Dong-Hua,Chen, Zhe-Sheng,Xu, Jinyi

, p. 993 - 1013 (2019/01/11)

A series of novel quinoline-chalcone der...

Quinoline formamide compound and preparation method thereof and application of anti-enterovirus type 71

-

Paragraph 0027-0030, (2020/01/03)

The invention discloses a quinoline form...

2388-32-1 Process route

2-chloroquinoline-4-carboxylic acid
5467-57-2

2-chloroquinoline-4-carboxylic acid

2-chloroquinoline-4-carbonyl chloride
2388-32-1

2-chloroquinoline-4-carbonyl chloride

Conditions
Conditions Yield
With thionyl chloride; for 1h; Heating;
With thionyl chloride; for 1h; Heating;
With thionyl chloride; N,N-dimethyl-formamide; In tetrahydrofuran; at 0 - 60 ℃; for 2h;
With oxalyl dichloride; N,N-dimethyl-formamide; In dichloromethane; at 20 ℃;
With thionyl chloride; Reflux;
With thionyl chloride; for 2h; Inert atmosphere; Reflux;
With oxalyl dichloride; N,N-dimethyl-formamide; In dichloromethane; at 0 - 20 ℃; for 1h;
With thionyl chloride; N,N-dimethyl-formamide; In dichloromethane; at 55 ℃; for 4h;
With thionyl chloride; In dichloromethane; at 55 ℃; for 4h;
2-hydroxyquinoline-4-carboxylic acid
15733-89-8,84906-81-0

2-hydroxyquinoline-4-carboxylic acid

2-chloroquinoline-4-carbonyl chloride
2388-32-1

2-chloroquinoline-4-carbonyl chloride

Conditions
Conditions Yield
With phosphorus pentachloride; chlorine; 1,2-dichloro-ethane;
With thionyl chloride; benzene;
With phosphorus pentachloride;
With phosphorus pentachloride; trichlorophosphate; for 18h; Heating / reflux;
With trichlorophosphate; at 100 ℃; for 1h;
With phosphorus pentachloride; trichlorophosphate;
With thionyl chloride; In 1,2-dichloro-ethane; at 80 ℃; for 2h;
With thionyl chloride; N,N-dimethyl-formamide; In dichloromethane; for 3h; Inert atmosphere; Resolution of racemate;
With thionyl chloride; In N,N-dimethyl-formamide; for 5h; Reflux;

2388-32-1 Upstream products

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    15733-89-8

    2-hydroxyquinoline-4-carboxylic acid

  • 5467-57-2
    5467-57-2

    2-chloroquinoline-4-carboxylic acid

  • 15733-89-8
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    2-quinolone-4-carboxylic acid

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    indole-2,3-dione

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    1-(2-chloro-quinoline-4-carbonyl)-4-phenyl-piperazine

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    2-(n-butyloxy)-4-(n-butyloxycarbonyl)-quinoline

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