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Catalog Number:
45367
CAS Number:
329-15-7
Chlorure de 4-(trifluorométhyl)benzoyle
Purity:
≥ 97% (CG)
Synonym(s):
Chlorure d'α,α,α-trifluoro- p -toluoyle
Hazmat
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Product Information

4-(Trifluoromethyl)benzoyl chloride is a highly versatile chemical compound recognized for its unique trifluoromethyl group, which enhances its reactivity and stability. This compound is widely utilized in the synthesis of various pharmaceuticals and agrochemicals, serving as a key intermediate in the production of fluorinated compounds. Its ability to introduce trifluoromethyl groups into organic molecules makes it invaluable in medicinal chemistry, where it can significantly improve the biological activity and metabolic stability of drug candidates. Additionally, 4-(Trifluoromethyl)benzoyl chloride is employed in the development of advanced materials and specialty chemicals, providing researchers with a powerful tool for creating innovative solutions in diverse applications.

With its distinct properties, 4-(Trifluoromethyl)benzoyl chloride stands out among similar compounds, offering enhanced performance in chemical reactions and greater efficiency in synthesis processes. Its role in the pharmaceutical industry, particularly in the design of new therapeutic agents, underscores its importance in modern chemistry. Researchers and industry professionals can leverage this compound to streamline their workflows and achieve superior results in their projects.

Synonyms
Chlorure d'α,α,α-trifluoro- p -toluoyle
CAS Number
329-15-7
Purity
≥ 97% (CG)
Molecular Formula
C8H4ClF3O
Molecular Weight
208.56
MDL Number
MFCD00000694
PubChem ID
67607
Melting Point
-3 °C
Density
1.41
Appearance
Liquide clair incolore à presque incolore
Boiling Point
68 °C/12 mmHg
Refractive Index
n20D 1.48
Conditions
Conserver entre 2 et 8 °C
General Information
Synonyms
Chlorure d'α,α,α-trifluoro- p -toluoyle
CAS Number
329-15-7
Purity
≥ 97% (CG)
Molecular Formula
C8H4ClF3O
Molecular Weight
208.56
MDL Number
MFCD00000694
PubChem ID
67607
Melting Point
-3 °C
Density
1.41
Appearance
Liquide clair incolore à presque incolore
Boiling Point
68 °C/12 mmHg
Refractive Index
n20D 1.48
Conditions
Conserver entre 2 et 8 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
Oui
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

4-(Trifluoromethyl)benzoyl chloride is widely utilized in research focused on:

  • Pharmaceutical Synthesis: This compound serves as a key intermediate in the production of various pharmaceuticals, particularly those requiring trifluoromethyl groups, which enhance biological activity and metabolic stability.
  • Agricultural Chemicals: It is used in the formulation of agrochemicals, including herbicides and pesticides, where the trifluoromethyl group contributes to improved efficacy and selectivity against pests.
  • Material Science: The compound is involved in the development of advanced materials, such as polymers and coatings, that benefit from its unique chemical properties, leading to enhanced durability and resistance to environmental factors.
  • Organic Synthesis: As a versatile reagent, it facilitates various organic transformations, making it valuable for chemists looking to create complex molecules efficiently.
  • Fluorinated Compounds: It plays a significant role in the synthesis of fluorinated compounds, which are important in numerous applications, including specialty chemicals and surfactants, due to their unique properties.

Citations