4-Chlorobutyryl chloride

  • CAS:4635-59-0
  • purity:99%
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Details

4-Chlorobutyryl chloride 4635-59-0 with purity >99% Low price in stock

  • Molecular Formula: C4H6Cl2O
  • Molecular Weight: 140.997
  • Appearance/Colour: colorless to light yellow liquid 
  • Vapor Pressure: 3 mm Hg ( 20 °C) 
  • Melting Point: -47 °C 
  • Refractive Index: 1.4610-1.4620 
  • Boiling Point: 174.3 °C at 760 mmHg 
  • Flash Point: 70.2 °C 
  • PSA: 17.07000 
  • Density: 1.231 g/cm3 
  • LogP: 1.77080 

4-Chlorobutyryl chloride(Cas 4635-59-0) Usage

Flammability and Explosibility

Nonflammable

InChI:InChI=1/C4H6Cl2O/c5-3-1-2-4(6)7/h1-3H2

4635-59-0 Relevant articles

-

Loftfield

, p. 1365 (1951)

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Intramolecular Cyclization of Brominated Oxime Ether Promoted with Ytterbium(0) to the Synthesis of Cyclic Imines

Wang, Yiqiong,Huang, Fei,Zhang, Songlin

supporting information, p. 5178 - 5181 (2020/08/13)

The first utility of ytterbium(0) as a m...

Monoterpenoid-based inhibitors of filoviruses targeting the glycoprotein-mediated entry process

Baev, Dmitriy S.,Maksyutov, Rinat A.,Mordvinova, Ekaterina D.,Pyankov, Oleg V.,Salakhutdinov, Nariman F.,Shcherbakov, Dmitriy N.,Shcherbakova, Nadezhda S.,Sokolova, Anastasiya S.,Tolstikova, Tatyana G.,Yarovaya, Olga I.,Zaykovskaya, Anna V.,Zybkina, Anastasiya V.

, (2020/09/09)

In this study, we screened a large libra...

FGFR INHIBITOR AND APPLICATION THEREOF

-

Paragraph 0249-0250, (2020/01/22)

An azatricyclic compound (as represented...

Method for long-term stable preparation of 4-chlorobutyryl chloride

-

Paragraph 0042-0068, (2020/08/27)

The invention relates to a synthesis met...

4635-59-0 Process route

4-butanolide
96-48-0

4-butanolide

4-Chlorobutanoyl chloride
4635-59-0

4-Chlorobutanoyl chloride

Conditions
Conditions Yield
With bis(trichloromethyl) carbonate; Al(3+)*3H2O4P(1-)*CH5N; In toluene; at 80 ℃; for 3h; Solvent; Reagent/catalyst; Large scale;
94.1%
With thionyl chloride; zinc(II) chloride; at 55 ℃; for 12h;
74%
With thionyl chloride; zinc(II) chloride; at 55 ℃; for 12h;
74%
With thionyl chloride; zinc(II) chloride; for 6h; Heating;
70%
With thionyl chloride; zinc(II) chloride; at 55 ℃; for 22h;
65%
With hydrogenchloride; anschliessend mit Thionylchlorid;
With thionyl chloride; zinc(II) chloride;
With phosphorus pentachloride; zinc(II) chloride;
With thionyl chloride; zinc(II) chloride; at 60 - 70 ℃;
With thionyl chloride; sulfuric acid;
With thionyl chloride; zinc(II) chloride;
With thionyl chloride; for 2h; Heating;
With thionyl chloride; zinc(II) chloride; Heating;
With thionyl chloride; zinc(II) chloride; Heating;
With Dichloromethyl methyl ether; zinc(II) chloride; at 60 ℃; for 2h;
With phosgene;
With thionyl chloride; zinc(II) chloride; at 60 ℃; for 5h;
γ-chlorobutyric acid
627-00-9

γ-chlorobutyric acid

4-Chlorobutanoyl chloride
4635-59-0

4-Chlorobutanoyl chloride

Conditions
Conditions Yield
With thionyl chloride; Heating;
97%
With thionyl chloride; In benzene; for 0.5h; Heating; water-bath;
58%
With thionyl chloride;
With thionyl chloride; Petroleum ether;
With phosphorus pentachloride;
With thionyl chloride; In dichloromethane; at 20 ℃; for 16h;
With thionyl chloride; In ethanol; at 0 ℃; for 2h; Reflux;
With thionyl chloride; In N,N-dimethyl-formamide; at 70 ℃; for 1.5h;
With thionyl chloride; at 25 ℃; for 2h; Reflux;
With oxalyl dichloride; In dichloromethane; at 0 - 20 ℃; for 2h;
With oxalyl dichloride; N,N-dimethyl-formamide; In dichloromethane; Inert atmosphere;
With thionyl chloride; at 100 ℃; for 4h; Inert atmosphere;
With oxalyl dichloride; N,N-dimethyl-formamide; In dichloromethane; at 20 ℃; for 4h; Inert atmosphere;
With thionyl chloride; for 2h; Reflux;
With thionyl chloride; for 2h; Reflux; Inert atmosphere;
With oxalyl dichloride; N,N-dimethyl-formamide; In dichloromethane; at 20 ℃; for 4h; Inert atmosphere;
With oxalyl dichloride; N,N-dimethyl-formamide; In dichloromethane; at 0 - 20 ℃; for 1h;

4635-59-0 Upstream products

  • 96-48-0
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    4-butanolide

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    tetrachloromethane

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    phosgene

  • 4885-02-3
    4885-02-3

    Dichloromethyl methyl ether

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    N-(p-tolyl)-4-chlorobutyramide

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