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Catalog Number:
31457
CAS Number:
37595-74-7
N-Phényl-bis(trifluorométhanesulfonimide)
Purity:
≥ 99 % (HPLC)
Synonym(s):
1,1,1-Trifluoro- N -phényl-N-[(trifluorométhyl)sulfonyl]méthanesulfonamide, N , N -Bis(trifluorométhylsulfonyl)aniline
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Product Information

N-Phenyl-bis(trifluoromethanesulfonimide) is a highly versatile compound known for its exceptional thermal stability and strong electrophilic properties. This compound is particularly valuable in the field of organic synthesis, where it serves as a powerful reagent for the introduction of trifluoromethyl groups into various organic molecules. Its unique structure allows for efficient reactions, making it a preferred choice among researchers and industry professionals looking to enhance the functionality of their compounds.

In addition to its synthetic applications, N-Phenyl-bis(trifluoromethanesulfonimide) is also utilized in the development of advanced materials, including polymers and pharmaceuticals. Its ability to facilitate complex chemical transformations while maintaining stability under harsh conditions makes it an essential tool in both academic and industrial laboratories. This compound stands out due to its low toxicity and high efficiency, offering a safer alternative compared to other trifluoromethylating agents. Whether you are working on drug development or material science, N-Phenyl-bis(trifluoromethanesulfonimide) is an invaluable asset that can significantly enhance your research outcomes.

Synonyms
1,1,1-Trifluoro- N -phényl-N-[(trifluorométhyl)sulfonyl]méthanesulfonamide, N , N -Bis(trifluorométhylsulfonyl)aniline
CAS Number
37595-74-7
Purity
≥ 99 % (HPLC)
Molecular Formula
C 8 H 5 F 6 NON 4 S 2
Molecular Weight
357.25
MDL Number
MFCD00000404
PubChem ID
142176
Melting Point
100 - 104 ?C
Appearance
Solide cristallin blanc à jaune clair
Conditions
Conserver à 0 - 8 °C
General Information
Synonyms
1,1,1-Trifluoro- N -phényl-N-[(trifluorométhyl)sulfonyl]méthanesulfonamide, N , N -Bis(trifluorométhylsulfonyl)aniline
CAS Number
37595-74-7
Purity
≥ 99 % (HPLC)
Molecular Formula
C 8 H 5 F 6 NON 4 S 2
Molecular Weight
357.25
MDL Number
MFCD00000404
PubChem ID
142176
Melting Point
100 - 104 ?C
Appearance
Solide cristallin blanc à jaune clair
Conditions
Conserver à 0 - 8 °C
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

N-Phenyl-bis(trifluoromethanesulfonimide) is widely utilized in research focused on:

  • Electrolyte Solutions: This compound serves as an effective electrolyte in lithium-ion batteries, enhancing their performance and stability, which is crucial for the energy storage industry.
  • Catalysis: It acts as a catalyst in various organic reactions, improving reaction rates and yields, making it valuable in pharmaceutical and fine chemical synthesis.
  • Fluorinated Polymers: The compound is used in the production of fluorinated polymers, which are known for their chemical resistance and thermal stability, benefiting industries such as coatings and materials science.
  • Ion-Selective Membranes: It is employed in the development of ion-selective membranes for sensors and separation technologies, enhancing the accuracy and efficiency of analytical devices.
  • Research and Development: This chemical is significant in academic and industrial research settings for developing new materials and exploring novel chemical pathways, fostering innovation in various scientific fields.

Citations