English

3′,5′-DICHLORO-2,2,2-TRIFLUOROACETOPHENONE

CAS NO.:130336-16-2

Purity: ≥98%

Appearance:Colorless to light yellow clear liquid

Product name 3′,5′-DICHLORO-2,2,2-TRIFLUOROACETOPHENONE
Synonym

3′,5′-DICHLORO-2,2,2-TRIFLUOROACETOPHENONE;1-(3,5-DICHLORO-PHENYL)-2,2,2-TRIFLUORO-ETHANONE;1-(3,5-dichlorophenyl)-2,2,2-trifluoro-1-ethanonChemicalbooke;1-(3,5-dichlorophenyl)-2,2,2-trifluoroethan-1-one;1-(3,5-DichL;uoroethanone;Ethanone,1-(3,5-dichlorophenyl)-2,2,2-trifluoro-;)-2,2,2-trifL

CAS NO. 130336-16-2
Appearance Colorless to light yellow clear liquid
Purity 98%
MF C8H3Cl2F3O
MW 243.01
Related categories Pharmaceutical Intermediates
Storage Keep in dark place,sealed in dry,room temperature
Transport Information Non-dangerous goods
HS Code(in China) 2914790090
Contact information Name:Echo Liu
E-mail:echo@coreychem.com

3′,5′-Dichloro-2,2,2-trifluoroacetophenone is a halogenated trifluoromethyl ketone compound widely utilized in pharmaceutical, agrochemical, and advanced materials research. With both electron-withdrawing trifluoromethyl and chlorine substituents on the aromatic ring, this compound exhibits high chemical reactivity and functional versatility, making it a valuable building block in synthetic organic chemistry.


⚗️ 1. Intermediate for Pharmaceutical Synthesis

This compound serves as a key intermediate in the synthesis of fluorinated drug molecules, particularly those targeting inflammation, oncology, and central nervous system disorders. The presence of the trifluoromethyl group enhances metabolic stability, lipophilicity, and bioavailability, while the dichlorinated phenyl ring contributes to binding specificity in drug-receptor interactions. It is frequently used in the preparation of:

  • Heterocyclic APIs

  • Trifluoromethylated aromatic scaffolds

  • Prodrug derivatives


🌾 2. Application in Agrochemical Development

In the agrochemical industry, 3′,5′-Dichloro-2,2,2-trifluoroacetophenone is explored as a precursor to herbicides, fungicides, and insecticides. Its structure enables selective binding to biological targets in pest organisms. The electron-deficient carbonyl and halogenated ring also offer potential sites for further modification, allowing fine-tuning of biological activity and environmental persistence.


🧪 3. Role in Specialty Chemical and Material Science

Beyond pharma and agrochemicals, this compound is applicable in specialty fluorinated materials, photoactive compounds, and electronic chemical synthesis. Its trifluoromethyl ketone moiety is known to participate in perfluoroalkylation reactions, making it useful in the preparation of high-performance polymers and liquid crystal materials.


⚠️ Handling Considerations

Due to its reactive ketone and halogen groups, 3′,5′-Dichloro-2,2,2-trifluoroacetophenone should be handled under controlled conditions using appropriate protective equipment. It should be stored in a tightly sealed container away from light and moisture.

●Product Manager Email: Echo@coreychem.com

Packaging:

Sample: 100g/bottle
Bulk: 50 kg/ drum

Customized packaging available upon request.

 

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