āĻĒ⧃āĻˇā§āĻ āĻž āύāĻŋāĻ°ā§āĻŦāĻžāϚāύ āĻ•āϰ⧁āύ

āĻĒāĻŖā§āϝ

Dichloroacetyl Chloride

  • āĻĒāĻŖā§āϝ⧇āϰ āύāĻžāĻŽ: āĻĄāĻžāχāĻ•ā§āϞ⧋āϰ⧋āϏ⧇āϏāĻŋāϟāĻžāχāϞ āĻ•ā§āϞ⧋āϰāĻžāχāĻĄ
  • āϏāĻŋ āĻ āĻāϏ āύāĻ‚.: 79-36-7
  • āĻŦāĻŋāĻļ⧁āĻĻā§āϧāϤāĻž: 99%
  • āĻāĻŽāĻāĻĢ: C2HCl3O
  • āĻšā§‡āĻšāĻžāϰāĻž: colorless fuming liquid
  • āĻĒā§āϝāĻžāϕ⧇āϜ: āĻŦā§āϝāĻžāĻ—
  • āϏāύāĻĻāĻĒāĻ¤ā§āϰ: āφāχāĻāϏāĻ“
  • āφāĻŦ⧇āĻĻāύ: It is a chemical compound primarily used in the synthesis of pharmaceuticals and agrochemicals. It is a reagent in organic chemistry that is utilized for various reactions, including the introduction of the dichloroacetyl group into molecules.
  • āύāĻŽā§āύāĻž: āĻĒāĻžāĻ“āϝāĻŧāĻž āϝāĻžāϝāĻŧ

āφāĻŽāĻžāĻĻ⧇āϰ āχāĻŽā§‡āχāϞ āĻĒāĻžāĻ āĻžāύ

āĻĒāĻŖā§āϝ āĻŦāĻŋāĻŦāϰāĻŖā§€

Dichloroacetyl chloride is an organic compound with the formula C2H2Cl2O. It is a colorless to yellowish liquid with a pungent odor. Chemical dichloroacetyl chloride is an important intermediate in organic synthesis and has been widely used in chemical synthesis and organic synthesis. It has electrophilic properties, especially suitable for alkylation, esterification, acylation and other reactions.
 

āĻĒāĻŖā§āϝ āĻĒāϰāĻžāĻŽāĻŋāϤāĻŋ

āϰāĻžāϏāĻžāϝāĻŧāύāĻŋāĻ• āϏ⧂āĻ¤ā§āϰ C2HCl3O āϏāĻŋ.āĻ.āĻāϏ. āύāĻŽā§āĻŦāϰ 79-36-7
āĻĒ⧇āώāĻ• āĻ­āϰ 147.38 g¡mol−1 āĻāĻ•āϟāĻŋ āϏāĻ‚āĻ–ā§āϝāĻž 1765
āĻŦ⧈āĻļāĻŋāĻˇā§āĻŸā§āϝ
āĻšā§‡āĻšāĻžāϰāĻž colorless fuming liquid
āϘāύāĻ¤ā§āĻŦ 1.5315 g/cm3
āĻ—āϞāύāĻžāĻ™ā§āĻ• <25 °āϏ⧇
āĻ¸ā§āĻĢ⧁āϟāύāĻžāĻ™ā§āĻ• 107 °āϏ⧇ (225 °āĻĢāĻž; 380 āϕ⧇)
āĻĒā§āϰāϤāĻŋāϏāϰāĻžāĻ™ā§āĻ• n20/D 1.46(āφāϞ⧋)
āĻĢā§āĻ˛ā§āϝāĻžāĻļ āĻĒāϝāĻŧ⧇āĻ¨ā§āϟ 66 °āϏ⧇
āĻĻā§āϰāĻžāĻŦā§āϝāϤāĻž Chloroform, Hexanes
āϏāĻ‚āĻŦ⧇āĻĻāύāĻļā§€āϞāϤāĻž Moisture Sensitive
āĻ¸ā§āĻŸā§‹āϰ⧇āϜ āĻ…āĻŦāĻ¸ā§āĻĨāĻž 2-8°āϏ⧇
āĻ¸ā§āĻĨāĻŋāϤāĻŋāĻļā§€āϞāϤāĻž āĻ¸ā§āĻĨāĻŋāϤāĻŋāĻļā§€āϞ. āĻĻāĻšāύāϝ⧋āĻ—ā§āϝ. Incompatible with water, alcohols and oxidizing agents. Fumes in air.

 

āφāĻŦ⧇āĻĻāύ

1. Drug synthesis: dichloroacetyl chloride is commonly used in the synthesis of drugs and bioactive compounds. It can react with amino acids, amines and alcohols to form various organic synthesis intermediates and drugs.

2. Esterification reaction: dichloroacetyl chloride can be used as a reagent for esterification reaction to react with alcohol to produce ester compounds, which are widely used in organic synthesis.

3. Nucleophilic substitution reaction: dichloroacetyl chloride can be substituted with nucleophilic reagents such as amino acids, mercaptans, āχāĻ¤ā§āϝāĻžāĻĻāĻŋ, to generate compounds with specific structures and activities.

4. Reagents and catalysts: dichloroacetyl chloride can be used as reagents and catalysts for catalytic and accelerator in some organic reactions.
 

āĻĒāĻŖā§āϝ⧇āϰ āĻāĻ•āĻžāϧāĻŋāĻ• āĻŦā§āϝāĻŦāĻšāĻžāϰ

āĻāϟāĻŋ āϰāĻžāϏāĻžāϝāĻŧāύāĻŋāĻ• āωāĻ¤ā§āĻĒāĻžāĻĻāύ āĻŦā§āϝāĻŦāĻšāĻžāϰ,āĻ”āώāϧ āĻļāĻŋāĻ˛ā§āĻĒ,āϰāĻžāϏāĻžāϝāĻŧāύāĻŋāĻ• āĻ—āĻŦ⧇āώāĻŖāĻž āĻ“ āωāĻ¨ā§āύāϝāĻŧāύ,Rubber and Plastics Modification

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