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Cyclobutanecarbonyl chloride

  • CasNo:5006-22-4

Product Description

Chemical plants supply high-quality Cyclobutanecarbonyl chloride 5006-22-4 in bulk

  • Molecular Formula: C5H7ClO
  • Molecular Weight: 118.563
  • Appearance/Colour: clear colourless liquid 
  • Vapor Pressure: 7.98mmHg at 25°C 
  • Melting Point: 151-152 °C 
  • Refractive Index: n20/D 1.455(lit.)  
  • Boiling Point: 134.7 °C at 760 mmHg 
  • Flash Point: 42.5 °C 
  • PSA: 17.07000 
  • Density: 1.22 g/cm3 
  • LogP: 1.55190 

Cyclobutanecarbonyl chloride(Cas 5006-22-4) Usage

InChI:InChI=1/C5H7ClO/c6-5(7)4-2-1-3-4/h4H,1-3H2

5006-22-4 Relevant articles

A new approach to substituted cyclobutanes: Direct β-deprotonation/magnesiation of cyclobutane carboxamides

Eaton, Philip E.,Zhang, Mao-Xi,Komiya, Naruyoshi,Yang, Cai-Guang,Steele, Ian,Gilardi, Richard

, p. 1275 - 1278 (2003)

BuMgN(i-Pr)2 is shown to be kinetically ...

SUBSTITUTED [1,2,4]TRIAZOLE COMPOUNDS AS FUNGICIDES

-

Page/Page column 98, (2021/12/31)

The present invention relates to substit...

Synthesis of N-trifluoromethyl amides from carboxylic acids

Flavell, Robert R.,Liu, Jianbo,Parker, Matthew F. L.,Toste, F. Dean,Wang, Sinan,Wilson, David M.

supporting information, p. 2245 - 2255 (2021/08/12)

Found in biomolecules, pharmaceuticals, ...

SUBSTITUTED AMINO TRIAZOLOPYRIMIDINE AND AMINO TRIAZOLOPYRAZINE ADENOSINE RECEPTOR ANTAGONISTS, PHARMACEUTICAL COMPOSITIONS AND THEIR USE

-

Page/Page column 58; 81, (2020/06/10)

In its many embodiments, the present inv...

Isoalantolactone derivative, pharmaceutical composition and application thereof

-

Paragraph 0014, (2019/02/02)

The invention relates to an isoalantolac...

5006-22-4 Process route

Cyclobutanecarboxylic acid
3721-95-7

Cyclobutanecarboxylic acid

Cyclobutanecarbonyl chloride
5006-22-4

Cyclobutanecarbonyl chloride

Conditions
Conditions Yield
With thionyl chloride; In toluene; Heating;
100%
With thionyl chloride; at 0 - 90 ℃; for 1.5h; Large scale;
48.9%
With phosphorus trichloride;
With thionyl chloride;
With thionyl chloride;
With thionyl chloride; In benzene;
With thionyl chloride; for 1h; Heating;
With thionyl chloride; In dichloromethane; at 20 ℃;
In thionyl chloride;
In thionyl chloride;
With oxalyl dichloride; In N,N-dimethyl-formamide; for 1.5h; Reflux;
With oxalyl dichloride; In dichloromethane; at 0 - 20 ℃; Inert atmosphere;
With oxalyl dichloride; In dichloromethane; N,N-dimethyl-formamide; at 20 ℃;
With thionyl chloride; at 0 ℃; for 1.5h; Reflux;
With oxalyl dichloride; In dichloromethane; N,N-dimethyl-formamide; at 0 - 20 ℃; for 5h; Inert atmosphere;
With oxalyl dichloride; N,N-dimethyl-formamide; In dichloromethane; at 0 - 20 ℃; for 1h;
With oxalyl dichloride; N,N-dimethyl-formamide; In dichloromethane; at 20 ℃;
With pyridine; oxalyl dichloride; In dichloromethane; N,N-dimethyl-formamide; at 0 - 20 ℃; for 4h; Inert atmosphere;
With thionyl chloride;
With oxalyl dichloride; N,N-dimethyl-formamide; In dichloromethane; Inert atmosphere;
With oxalyl dichloride; In dichloromethane; N,N-dimethyl-formamide; at 24 ℃; Inert atmosphere;
With oxalyl dichloride; N,N-dimethyl-formamide; In dichloromethane; at 0 - 20 ℃; for 1.5h; Inert atmosphere;
With oxalyl dichloride; N,N-dimethyl-formamide; In dichloromethane; for 2h;
With oxalyl dichloride; In dichloromethane; N,N-dimethyl-formamide; for 2h;
With thionyl chloride; In dichloromethane; for 6h; Reflux;
With oxalyl dichloride; N,N-dimethyl-formamide; In dichloromethane; at 0 - 40 ℃; for 10h;
With oxalyl dichloride; N,N-dimethyl-formamide; In dichloromethane; at 35 ℃; for 1.5h; Inert atmosphere;
With oxalyl dichloride; N,N-dimethyl-formamide; In dichloromethane; at 0 ℃; for 2h; Inert atmosphere;
With oxalyl dichloride; N,N-dimethyl-formamide; In dichloromethane; at 0 - 20 ℃;
thionyl chloride
7719-09-7

thionyl chloride

Cyclobutanecarboxylic acid
3721-95-7

Cyclobutanecarboxylic acid

Cyclobutanecarbonyl chloride
5006-22-4

Cyclobutanecarbonyl chloride

Conditions
Conditions Yield
With N,N-dimethyl-formamide; In tetrahydrofuran; at 20 ℃; for 2h;

5006-22-4 Upstream products

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    diethyl cyclobutane-1,1-dicarboxylate

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5006-22-4 Downstream products

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  • 14924-53-9
    14924-53-9

    ethyl cyclobutylcarboxylate

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    Cyclobutancarbonsaeure-cyclopropylmethylester

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    5407-98-7

    1-cyclobutyl-1-phenyl-methanone

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