CAS 37595-74-7

N-feniltrifluorometansulfonimmide

Descrizione:

N-feniltrifluorometansulfonimmide, con il numero CAS 37595-74-7, è un composto sulfonamide caratterizzato dalla presenza di un gruppo trifluorometanosulfonile attaccato a un anello fenilico. Questo composto è noto per la sua alta stabilità termica e ottima solubilità in solventi aprotici polari, rendendolo utile in varie applicazioni chimiche, in particolare nella sintesi organica e come reagente nella preparazione di liquidi ionici. Il suo gruppo trifluorometile contribuisce alle sue forti proprietà di attrazione elettronica, migliorando la sua reattività nelle reazioni di sostituzione nucleofila. Inoltre, N-feniltrifluorometansulfonimmide presenta bassa tossicità ed è considerato un solido non igroscopico, il che è vantaggioso per la manipolazione e lo stoccaggio. Le proprietà uniche del composto lo rendono uno strumento prezioso nello sviluppo di nuovi materiali e nel campo della catalisi, dove può facilitare varie trasformazioni chimiche. In generale, le sue caratteristiche distintive lo posizionano come un composto significativo sia nella ricerca accademica che nelle applicazioni industriali.

Formula: 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

InChI key: InChIKey=DIOHEXPTUTVCNX-UHFFFAOYSA-N

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

Sinonimi:

• 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) [Triflating Reagent]

CAS: 37595-74-7

Formula: C₈H₅F₆NO₄S₂

Purezza: >98.0%(GC)

Colore e forma: White to Almost white powder to crystal

Peso molecolare: 357.24

Ref: 3B-P1257

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

Formula: C₈H₅F₆NO₄S₂

Purezza: 99%

Colore e forma: White to pale cream, crystalline solid

Peso molecolare: 357.24

Ref: 02-L12531

N,N-Bis(trifluoromethylsulfonyl)aniline

CAS: 37595-74-7

Formula: C₈H₅F₆NO₄S₂

Purezza: 96%

Colore e forma: Solid

Peso molecolare: 357.2500

Ref: IN-DA0035B0

N,N-Bis(trifluoromethylsulphonyl)aniline

CAS: 37595-74-7

N,N-Bis(trifluoromethylsulphonyl)aniline

Formula: C₈H₅F₆NO₄S₂

Purezza: 98%

Colore e forma: beige solid

Peso molecolare: 357.25g/mol

Ref: 54-PC6227

N-Phenyl-bis(trifluoromethanesulfonimide)

CAS: 37595-74-7

Formula: C₈H₅F₆NO₄S₂

Purezza: ≥ 97.0%

Colore e forma: White to off-white crystalline powder

Peso molecolare: 357.25

Ref: 7W-GX3512

N-Phenyl bis-trifluoromethane sulfonimide

CAS: 37595-74-7

Formula: C₈H₅F₆NO₄S₂

Purezza: 98.0%

Colore e forma: Solid, Chunks or Crystalline Powder

Peso molecolare: 357.24

Ref: 10-F024773

N-Phenylbis(trifluoromethanesulfonamide)

Prodotto controllato

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);

Formula: C₈H₅F₆NO₄S₂

Colore e forma: Neat

Peso molecolare: 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.

Formula: C₈H₅F₆NO₄S₂

Purezza: Min. 95%

Colore e forma: White Powder

Peso molecolare: 357.25 g/mol

Ref: 3D-FP11247