CAS 37595-74-7

N-feniltrifluorometanosulfonimida

Descripción:

N-feniltrifluorometanosulfonimida, con el número CAS 37595-74-7, es un compuesto sulfonamida caracterizado por la presencia de un grupo trifluorometanosulfonilo unido a un anillo fenílico. Este compuesto es conocido por su alta estabilidad térmica y excelente solubilidad en disolventes aproticos polares, lo que lo hace útil en diversas aplicaciones químicas, particularmente en la síntesis orgánica y como reactivo en la preparación de líquidos iónicos. Su grupo trifluorometilo contribuye a sus fuertes propiedades de atracción electrónica, mejorando su reactividad en reacciones de sustitución nucleofílica. Además, N-feniltrifluorometanosulfonimida exhibe baja toxicidad y se considera un sólido no higroscópico, lo que es ventajoso para su manejo y almacenamiento. Las propiedades únicas del compuesto lo convierten en una herramienta valiosa en el desarrollo de nuevos materiales y en el campo de la catálisis, donde puede facilitar diversas transformaciones químicas. En general, sus características distintivas lo posicionan como un compuesto significativo tanto en la investigación académica como en aplicaciones industriales.

Fórmula: C₈H₅F₆NO₄S₂

InChI: InChI=1S/C8H5F6NO4S2/c9-7(10,11)20(16,17)15(6-4-2-1-3-5-6)21(18,19)8(12,13)14/h1-5H

Clave InChI: InChIKey=DIOHEXPTUTVCNX-UHFFFAOYSA-N

SMILES: N(S(C(F)(F)F)(=O)=O)(S(C(F)(F)F)(=O)=O)C1=CC=CC=C1

Sinónimos:

• 1,1,1-Trifluoro-N-phenyl-N-trifluoromethanesulfonylmethanesulfonamide
• 1,1,1-trifluoro-N-phenyl-N-[(trifluoromethyl)sulfonyl]methanesulfonamide
• Methanesulfonamide, 1,1,1-trifluoro-N-phenyl-N-[(trifluoromethyl)sulfonyl]-
• N,N-Bis(trifluoromethanesulfonyl)aniline
• N,N-Bis(trifluoromethanesulphonyl)aniline
• N,N-Bis(trifluoromethylsulfonyl)aniline
• N,N-Bis(trifluoromethylsulfonyl)phenylamine
• N-Phenyl-N-(trifluoromethanesulfonyl)trifluoromethanesulfonamide
• N-Phenyl-N-[(trifluoromethyl)sulfonyl]trifluoromethanesulfonamide
• N-Phenyl-bis(trifluoromethanesulfonimide)
• N-Phenylbis(trifluoromethanesulfonimide)
• N-Phenylbis(trifluoromethanesulfonyl)imide
• N-Phenyltriflimide
• N-Phenyltrifluoromethanesulfonimide
• N-Phenyltrifluoromethanesulphonimide
• N-Phenyltrifluoromethylsulfonimide
• N-phenyl-bis (trifluoromethanesulfonyl) imide
• NSC 240874
• PhNTf₂
• Phenyl bis((trifluoromethyl)sulfonyl)amine
• Phenyl triflimide

N-Phenylbis(trifluoromethanesulfonimide), 99%

CAS: 37595-74-7

N-Phenylbis(trifluoromethanesulfonimide) acts as a mild triflating reagent as well as a transparent strong electron-withdrawing p-type dopant in carbon nanotubes. It is also employed as a reactant for the preparation of amphoteric alfa-boryl aldehydes. It plays an important role in the enantioselect

Fórmula: C₈H₅F₆NO₄S₂

Pureza: 99%

Forma y color: White to pale cream, crystalline solid

Peso molecular: 357.24

Ref: 02-L12531

N,N-Bis(trifluoromethylsulphonyl)aniline

CAS: 37595-74-7

N,N-Bis(trifluoromethylsulphonyl)aniline

Fórmula: C₈H₅F₆NO₄S₂

Pureza: 98%

Forma y color: Beige Solid-Crystals

Peso molecular: 357.25001

Ref: 54-PC6227

N,N-Bis(trifluoromethylsulfonyl)aniline

CAS: 37595-74-7

Fórmula: C₈H₅F₆NO₄S₂

Pureza: 98%

Forma y color: Solid

Peso molecular: 357.2500

Ref: IN-DA0035B0

N-Phenyl-bis(trifluoromethanesulfonimide)

CAS: 37595-74-7

Fórmula: C₈H₅F₆NO₄S₂

Pureza: ≥ 97.0%

Forma y color: White to off-white crystalline powder

Peso molecular: 357.25

Ref: 7W-GX3512

N-Phenyl bis-trifluoromethane sulfonimide

CAS: 37595-74-7

Fórmula: C₈H₅F₆NO₄S₂

Pureza: 98.0%

Forma y color: Solid, Chunks or Crystalline Powder

Peso molecular: 357.24

Ref: 10-F024773

N,N-Bis(trifluoromethylsulfonyl)aniline

CAS: 37595-74-7

1,1,1-Trifluoro-N-phenyl-N-((trifluoromethyl)sulfonyl)methanesulfonamide

Fórmula: C₈H₅F₆NO₄S₂

Pureza: 98%

Peso molecular: 357.25

Ref: IN-DG33456

N-Phenylbis(trifluoromethanesulfonamide)

Producto controlado

CAS: 37595-74-7

Stability Moisture Sensitive
Applications N-Phenylbis(trifluoromethanesulfonamide) is used in the enantioselective synthesis of β-amino acids via the Mannich reaction. Used in the synthesis of sphingosine 1-phosphate-1 receptor agonists useful in pharmaceutical application.
References Asano, M. et al.: Tetra. Asymm., 24, 449 (2013);

Fórmula: C₈H₅F₆NO₄S₂

Forma y color: Neat

Peso molecular: 357.25

Ref: TR-P319780

N-Phenylbistrifluoromethanesulfonimide

CAS: 37595-74-7

N-Phenylbistrifluoromethanesulfonimide (NPBF) is a nitro compound that has been synthesized in an asymmetric synthesis. The chemical stability of NPBF is advantageous for the preparation of fluorescence probes. It has been used to study the structure and function of proteins, such as dopamine receptors, which are important in autoimmune diseases and metabolic disorders. A x-ray diffraction data study of NPBF was performed on tissue culture cells with human serum. This compound has shown a high affinity for Jak2 V617F mutants and organic chemists have investigated its use as a palladium-catalyzed coupling agent.

Fórmula: C₈H₅F₆NO₄S₂

Pureza: Min. 95%

Forma y color: White Powder

Peso molecular: 357.25 g/mol

Ref: 3D-FP11247

N-Phenylbis(trifluoromethanesulfonimide) [Triflating Reagent]

CAS: 37595-74-7

Fórmula: C₈H₅F₆NO₄S₂

Pureza: >98.0%(GC)

Forma y color: White to Almost white powder to crystal

Peso molecular: 357.24

Ref: 3B-P1257