CAS 2993-22-8

(OC-6-21)-(3-Aminophenyl)pentafluorosulfur

Description:

(OC-6-21)-(3-Aminophenyl)pentafluorosulfur, with the CAS number 2993-22-8, is a specialized chemical compound that features a unique structure characterized by the presence of a pentafluorosulfur moiety. This compound typically exhibits high thermal and chemical stability due to the strong bonds formed by the fluorine atoms, which can enhance its reactivity in certain applications. The presence of the 3-aminophenyl group suggests potential for interactions in biological systems, making it of interest in medicinal chemistry and materials science. Its fluorinated nature may impart hydrophobic properties, influencing solubility and reactivity in various solvents. Additionally, the compound may exhibit unique electronic properties due to the electron-withdrawing effects of the fluorine atoms, which can affect its behavior in chemical reactions. Overall, (OC-6-21)-(3-Aminophenyl)pentafluorosulfur is a compound of interest for research and industrial applications, particularly in fields that explore fluorinated compounds and their derivatives.

Formula: C₆H₆F₅NS

InChI: InChI=1S/C6H6F5NS/c7-13(8,9,10,11)6-3-1-2-5(12)4-6/h1-4H,12H2

InChI key: InChIKey=NUFLICUHOXHWER-UHFFFAOYSA-N

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

Synonyms:

• (3-Aminophenyl)pentafluorosulfur
• (OC-6-21)-(3-Aminophenyl)pentafluorosulfur
• (m-Aminophenyl)sulfur pentafluoride
• 2993-22-8
• 3-(Aminophenyl)sulfur pentafluoride
• 3-(Pentafluoro-lambda6-sulfanyl)aniline
• 3-(Pentafluorosulfanyl)aniline
• 3-(Pentafluorosulfanyl)phenylamine
• 3-(Pentafluorosulfur)aniline
• 3-(Pentafluorothio)aniline
• 3-Amino(pentafluorosulfanyl)benzene
• 3-Aminophenylsulphur pentafluoride
• Aniline, m-pentafluorosulfur deriv.
• Sulfur, (3-Aminophenyl)Pentafluoro-
• Sulfur, (3-aminophenyl)pentafluoro-, (OC-6-21)-

3-(Pentafluorothio)aniline, 97%

CAS: 2993-22-8

Reduction of pentafluoroaniline (PFA) leads to rapid fluoride elimination to form the aminotetrafluorophenyl radical. Homolytic reactions of perfluoroaromatic compounds(Formation of pentafluorophenyl radicals from pentafluoroaniline, and their reactions with aromatic compounds). This Thermo Scientif

Formula: C₆H₆F₅NS

Purity: 97%

Color and Shape: White to pale cream to pale yellow, Crystals or powder or crystalline powder or clear liquid as melt

Molecular weight: 219.17

Ref: 02-H35190

3-(Pentafluorosulfur)aniline

CAS: 2993-22-8

Formula: C₆H₆F₅NS

Purity: 97%

Color and Shape: Liquid

Molecular weight: 219.1756

Ref: IN-DA00VRP9

3-Aminophenylsulphur pentafluoride

CAS: 2993-22-8

3-Aminophenylsulphur pentafluoride

Formula: C₆H₆F₅NS

Purity: 97%

Color and Shape: light brown crystals

Molecular weight: 219.18g/mol

Ref: 54-PC0779

3-Aminophenylsulphur pentafluoride

CAS: 2993-22-8

Formula: C₆H₆F₅NS

Purity: 97%

Color and Shape: Solid

Molecular weight: 219.17

Ref: 10-F050229

3-Aminophenylsulphur pentafluoride

CAS: 2993-22-8

3-Aminophenylsulphur pentafluoride is a synthetic chemical compound. It is a ligand with an electron-withdrawing group and has been shown to be a strong oxidizing agent. 3-Aminophenylsulphur pentafluoride reacts with phosphine oxides, yielding phosphines. This reaction can be used for the synthesis of heterocycles that contain phosphorus in their ring system. 3-Aminophenylsulphur pentafluoride also reacts with alkyl halides to produce heterocycles containing sulphur, such as pyridines or thiophenes. The reaction time between 3-aminophenylsulphur pentafluoride and alkyl halides is dependent on the oxidation potential of the alkyl halides, which can be determined by measuring the absorption spectra of the resulting heterocycles. 3-Aminophenylsulf

Formula: C₆H₆F₅NS

Purity: Min. 95%

Molecular weight: 219.18 g/mol

Ref: 3D-FA76566