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Catalog Number:
45558
CAS Number:
326-06-7
4,4,4-Trifluoro-1-phényl-1,3-butanedione
Purity:
≥ 98% (CG)
Synonym(s):
Benzoyltrifluoroacétone
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Product Information

4,4,4-Trifluoro-1-phenyl-1,3-butanedione is a versatile compound known for its unique trifluoromethyl group, which enhances its reactivity and stability in various chemical processes. This compound is widely utilized in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals. Its ability to act as a building block in the synthesis of complex molecules makes it invaluable for researchers looking to innovate in drug design and development. Additionally, its fluorinated structure contributes to improved solubility and bioavailability of active pharmaceutical ingredients, making it an attractive option for formulation scientists.

In the field of materials science, 4,4,4-Trifluoro-1-phenyl-1,3-butanedione serves as a key intermediate in the production of fluorinated polymers and coatings, which exhibit enhanced chemical resistance and thermal stability. This compound's unique properties allow for the creation of high-performance materials that can withstand harsh environments, making it essential for applications in electronics, automotive, and aerospace industries. With its broad range of applications and benefits, 4,4,4-Trifluoro-1-phenyl-1,3-butanedione is a valuable addition to any chemical toolkit.

Synonyms
Benzoyltrifluoroacétone
CAS Number
326-06-7
Purity
≥ 98% (CG)
Molecular Formula
C10H7F3O2
Molecular Weight
216.16
MDL Number
MFCD00000425
PubChem ID
67589
Melting Point
37 - 41 °C
Density
1.11
Appearance
Poudre blanche à orange à verte en grumeau
Boiling Point
224 °C
Conditions
Conserver entre 2 et 8 °C
General Information
Synonyms
Benzoyltrifluoroacétone
CAS Number
326-06-7
Purity
≥ 98% (CG)
Molecular Formula
C10H7F3O2
Molecular Weight
216.16
MDL Number
MFCD00000425
PubChem ID
67589
Melting Point
37 - 41 °C
Density
1.11
Appearance
Poudre blanche à orange à verte en grumeau
Boiling Point
224 °C
Conditions
Conserver entre 2 et 8 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

4,4,4-Trifluoro-1-phenyl-1,3-butanedione is widely utilized in research focused on:

  • Organic Synthesis: This compound serves as a versatile building block in organic chemistry, enabling the synthesis of various fluorinated compounds that are valuable in pharmaceuticals and agrochemicals.
  • Fluorinated Drug Development: Its unique trifluoromethyl group enhances the biological activity of drug candidates, making it a crucial component in the development of more effective pharmaceuticals.
  • Material Science: Used in the formulation of specialty polymers and coatings, it improves the thermal stability and chemical resistance of materials, which is essential in industries like electronics and automotive.
  • Analytical Chemistry: This compound acts as a reagent in analytical methods, helping researchers identify and quantify other substances, particularly in complex mixtures.
  • Research in Catalysis: It plays a significant role in catalytic processes, facilitating reactions that are critical for producing fine chemicals and intermediates in various industrial applications.

Citations