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Catalog Number:
45559
CAS Number:
893-33-4
4,4,4-Trifluoro-1-(2-naftil)-1,3-butanodiona
Purity:
≥ 98% (GC)
Synonym(s):
3-(2-naftoil)-1,1,1-trifluoroacetona
Documents
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Product Information

4,4,4-Trifluoro-1-(2-naphthyl)-1,3-butanedione is a highly versatile compound known for its unique trifluoromethyl group, which enhances its reactivity and stability in various chemical processes. This compound is particularly valuable in the synthesis of fluorinated organic compounds, making it an essential building block in pharmaceuticals and agrochemicals. Its distinctive structure allows for effective incorporation into complex molecular architectures, facilitating the development of innovative materials and functionalized products. Researchers and industry professionals can leverage its properties for applications in medicinal chemistry, where it may serve as a precursor for designing novel therapeutic agents.

Additionally, 4,4,4-Trifluoro-1-(2-naphthyl)-1,3-butanedione has shown promise in the field of organic electronics, particularly in the fabrication of organic light-emitting diodes (OLEDs) and other optoelectronic devices. Its ability to enhance charge transport and stability makes it a valuable candidate for improving device performance. With its unique characteristics and broad applicability, this compound stands out as a crucial resource for advancing research and development in various scientific fields.

Synonyms
3-(2-naftoil)-1,1,1-trifluoroacetona
CAS Number
893-33-4
Purity
≥ 98% (GC)
Molecular Formula
C14H9F3O2
Molecular Weight
266.22
MDL Number
MFCD00054501
PubChem ID
70179
Melting Point
73 - 76 °C
Appearance
Polvo blanco a casi blanco a cristal.
Conditions
Conservar entre 2 y 8 °C.
General Information
Synonyms
3-(2-naftoil)-1,1,1-trifluoroacetona
CAS Number
893-33-4
Purity
≥ 98% (GC)
Molecular Formula
C14H9F3O2
Molecular Weight
266.22
MDL Number
MFCD00054501
PubChem ID
70179
Melting Point
73 - 76 °C
Appearance
Polvo blanco a casi blanco a cristal.
Conditions
Conservar entre 2 y 8 °C.
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

4,4,4-Trifluoro-1-(2-naphthyl)-1,3-butanedione is widely utilized in research focused on:

  • Organic Synthesis: This compound serves as a versatile building block in the synthesis of various organic molecules, particularly in the development of pharmaceuticals and agrochemicals.
  • Fluorescent Probes: It is used in the creation of fluorescent probes for biological imaging, allowing researchers to visualize cellular processes with high sensitivity.
  • Material Science: The compound is incorporated into polymer formulations to enhance thermal stability and chemical resistance, making it valuable in the production of durable materials.
  • Analytical Chemistry: It acts as a reagent in analytical methods, aiding in the detection and quantification of other compounds, which is crucial for quality control in various industries.
  • Photovoltaic Applications: The compound is explored for its potential in organic solar cells, contributing to the development of sustainable energy solutions through improved light absorption and conversion efficiency.

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