CAS 76-02-8

2,2,2-Trichloroacetyl chloride

Description:

2,2,2-Trichloroacetyl chloride, with the CAS number 76-02-8, is an organic compound characterized by its structure, which includes a trichloroacetyl group attached to a chloride. It appears as a colorless to yellowish liquid with a pungent odor, indicative of its reactivity and potential hazards. This compound is known for its role as an acylating agent in organic synthesis, particularly in the preparation of various derivatives and intermediates. It is highly reactive, especially with water, leading to the formation of hydrochloric acid and trichloroacetic acid upon hydrolysis. Due to its corrosive nature, it poses significant health risks, including respiratory irritation and skin burns, necessitating careful handling and appropriate safety measures. Additionally, it is classified as a hazardous substance, and its use is regulated in many jurisdictions. Overall, 2,2,2-Trichloroacetyl chloride is a valuable reagent in chemical synthesis but requires stringent safety protocols due to its toxic and reactive properties.

Formula: C₂Cl₄O

InChI: InChI=1S/C2Cl4O/c3-1(7)2(4,5)6

InChI key: InChIKey=PVFOMCVHYWHZJE-UHFFFAOYSA-N

SMILES: C(C(Cl)=O)(Cl)(Cl)Cl

Synonyms:

• 2,2,2-Trichloroacetyl chloride
• Acetyl chloride, 2,2,2-trichloro-
• Chlorure de trichloroacetyle
• Cloruro De Tricloroacetilo
• Nsc 190466
• Trichlor-Acetylchlorid
• Trichloracetylchlorid
• Trichloroacetic acid chloride
• Trichloroacetochloride
• Trichloroacetyl Chloride
• Trichloroacetyl chloride [UN2442] [Corrosive]
• UN2442
• Acetyl chloride, trichloro-
• Superpalite
• HSDB 6321
• BRN 0774120

Trichloroacetyl chloride, 99%

CAS: 76-02-8

Trichloroacetyl chloride is used in the preparation of dihydro-1H-benzindoles. It is also used in the synthesis of 3-alkylbenzoxazolones It is used in the manufacture of pharmaceuticals and plant protection compounds. It is used for manufacturing the esters and anhydrides of trichloroacetic acid. I

Formula: C₂Cl₄O

Purity: 99%

Color and Shape: Clear colorless to pale yellow or pink, Liquid

Molecular weight: 181.82

Ref: 02-B21675

Trichloroacetyl chloride

CAS: 76-02-8

Formula: CCl₃COCl

Purity: (GC) ≥ 98.0%

Color and Shape: Clear, colourless to pale yellow liquid

Molecular weight: 181.83

Ref: 7W-GK1083

Trichloroacetyl chloride

CAS: 76-02-8

Trichloroacetyl chloride is an oxidation catalyst that is used for the synthesis of organic compounds. It is particularly useful in the synthesis of 2-chloropropane from chloropropane and sodium chloride in a reaction solution containing water vapor and hydrogen fluoride. Trichloroacetyl chloride has been shown to be an effective antimicrobial agent against a number of bacterial strains, including Staphylococcus aureus, Salmonella typhimurium, Escherichia coli, and Pseudomonas aeruginosa. This compound also has antibacterial activity against Mycobacterium tuberculosis and Streptococcus pneumoniae. The mechanism of action is not fully understood but may involve the release of chlorine gas and oxidation by oxygen radicals. Trichloroacetyl chloride has been shown to react with magnesium salts to form magnesium trichloride (MgCl2) in an analytical method called "magnesium titration." The reaction between trich

Formula: C₂Cl₄O

Purity: Min. 95%

Color and Shape: Clear Liquid

Molecular weight: 181.83 g/mol

Ref: 3D-FT34593

Trichloroacetyl Chloride

CAS: 76-02-8

Formula: C₂Cl₄O

Color and Shape: Colourless Oil

Molecular weight: 181.83

Ref: TR-T773935