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Catalog Number:
36577
CAS Number:
121287-02-3
N-(4-tert-Butylphenyl)bis(trifluoromethanesulfonimide)
Purity:
≥ 97% (GC)
Synonym(s):
N-[4-(1,1-Dimethylethyl)phenyl]-1,1,1-trifluoro-N-[(trifluoromethyl)sulfonyl]-methanesulfonamide
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Product Information

N-(4-tert-Butylphenyl)bis(trifluoromethanesulfonimide) is a highly versatile compound known for its exceptional thermal stability and strong ionic character, making it an ideal choice for various applications in the fields of organic synthesis and materials science. This compound serves as an effective electrolyte in lithium-ion batteries, enhancing their performance and longevity. Its unique structure allows for improved conductivity and efficiency, which is crucial for the development of advanced energy storage solutions. Additionally, it is utilized in the synthesis of specialty polymers and as a reagent in chemical reactions, providing researchers with a reliable tool for creating complex molecular architectures.

The compound's trifluoromethanesulfonimide moiety contributes to its high solubility in organic solvents, facilitating its use in diverse chemical environments. Its application in the production of ionic liquids further underscores its significance in green chemistry, where it aids in reducing environmental impact while maintaining high efficiency in chemical processes. With its robust properties and broad applicability, N-(4-tert-Butylphenyl)bis(trifluoromethanesulfonimide) stands out as a valuable asset for researchers and industry professionals seeking innovative solutions in energy and materials development.

Synonyms
N-[4-(1,1-Dimethylethyl)phenyl]-1,1,1-trifluoro-N-[(trifluoromethyl)sulfonyl]-methanesulfonamide
CAS Number
121287-02-3
Purity
≥ 97% (GC)
Molecular Formula
C12H13F6NO4S2
Molecular Weight
413.36
MDL Number
MFCD16875668
PubChem ID
15602477
Melting Point
108 - 112 °C
Appearance
White to off-white to yellowish crystalline powder
Conditions
Store at RT, under inert gas
General Information
Synonyms
N-[4-(1,1-Dimethylethyl)phenyl]-1,1,1-trifluoro-N-[(trifluoromethyl)sulfonyl]-methanesulfonamide
CAS Number
121287-02-3
Purity
≥ 97% (GC)
Molecular Formula
C12H13F6NO4S2
Molecular Weight
413.36
MDL Number
MFCD16875668
PubChem ID
15602477
Melting Point
108 - 112 °C
Appearance
White to off-white to yellowish crystalline powder
Conditions
Store at RT, under inert gas
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

N-(4-tert-Butylphenyl)bis(trifluoromethanesulfonimide) is widely utilized in research focused on:

  • Electrolytes in Energy Storage: This compound serves as an effective electrolyte in lithium-ion batteries, enhancing their performance and longevity. Its unique properties allow for better ionic conductivity, which is essential for efficient energy storage.
  • Advanced Coatings: It is used in formulating high-performance coatings that offer excellent thermal stability and chemical resistance. Industries such as automotive and aerospace benefit from these coatings to protect surfaces from harsh environments.
  • Fluorinated Solvents: The chemical acts as a solvent in various chemical reactions, particularly in fluorination processes. This application is crucial in pharmaceuticals and agrochemicals, where specific reactions require non-reactive solvents.
  • Polymer Production: It is utilized in the synthesis of specialty polymers that exhibit superior thermal and mechanical properties. These polymers find applications in electronics and medical devices, where reliability is critical.
  • Research in Organofluorine Chemistry: This compound is a valuable reagent in organofluorine synthesis, helping researchers develop new fluorinated compounds with potential applications in drug discovery and materials science.

Citations