CAS 832-53-1

2,3,4,5,6-Pentafluorobenzenesulfonyl chloride

Description:

2,3,4,5,6-Pentafluorobenzenesulfonyl chloride, with the CAS number 832-53-1, is a highly fluorinated aromatic sulfonyl chloride. This compound features a benzene ring substituted with five fluorine atoms and a sulfonyl chloride group, making it a potent electrophile. Its structure contributes to its high reactivity, particularly in nucleophilic substitution reactions, where it can act as a sulfonylating agent. The presence of multiple fluorine atoms enhances its stability and lipophilicity, while also imparting unique electronic properties that can influence its reactivity and interactions with other chemical species. This compound is typically used in organic synthesis, particularly in the preparation of sulfonamides and other fluorinated compounds. Due to its reactivity and the presence of chlorine, it should be handled with care, as it can be corrosive and may pose health hazards upon exposure. Proper safety measures, including the use of personal protective equipment and working in a fume hood, are essential when working with this substance.

Formula: C₆ClF₅O₂S

InChI: InChI=1S/C6ClF5O2S/c7-15(13,14)6-4(11)2(9)1(8)3(10)5(6)12

InChI key: InChIKey=UOJCTEGNHXRPKO-UHFFFAOYSA-N

SMILES: S(Cl)(=O)(=O)C1=C(F)C(F)=C(F)C(F)=C1F

Synonyms:

• 2,3,4,5,6-Pentafluorobenzene-1-sulfonyl chloride
• 2,3,4,5,6-Pentafluorobenzenesulfonyl chloride
• 2,3,4,5,6-Pentafluorophenylsulfonyl chloride
• Benzenesulfonyl chloride, 2,3,4,5,6-pentafluoro-
• Benzenesulfonyl chloride, pentafluoro-
• F05480 2,3,4,5,6-Pentafluorobenzenesulfonyl chloride
• NSC 96998
• Pentafluorobenzenesulphonyl chloride
• Pentafluorophenylsulfonyl chloride
• Pentafluororbenzenesulfonyl chloride
• Perfluorobenzenesulfonyl chloride

Pentafluorobenzenesulfonyl Chloride

CAS: 832-53-1

Formula: C₆ClF₅O₂S

Purity: >98.0%(GC)

Color and Shape: Colorless to Almost colorless clear liquid

Molecular weight: 266.57

Ref: 3B-P0934

Pentafluorobenzenesulfonyl chloride

CAS: 832-53-1

Formula: C₆ClF₅O₂S

Purity: 99.0%

Color and Shape: Clear

Molecular weight: 266.57

Ref: 10-F006949

2,3,4,5,6-Pentafluorobenzenesulfonyl chloride, 98+%

CAS: 832-53-1

Pentafluorobenzenesulfonyl chloride is used as derivatizing reagent for simultaneous determination of fluoxetine and p-trifluoromethylphenol, an O-dealkylated metabolite of fluoxetine in human liver microsomes. It is also used for electrophore labeling of small tyrosyl peptides for their analysis b

Formula: C₆ClF₅O₂S

Purity: 98+%

Color and Shape: Clear colorless to pale yellow, Liquid

Molecular weight: 266.57

Ref: 02-A17676

2,3,4,5,6-Pentafluorobenzene-1-sulfonyl chloride

CAS: 832-53-1

Formula: C₆ClF₅O₂S

Purity: 95%

Color and Shape: Liquid

Molecular weight: 266.5730

Ref: IN-DA003TLA

Pentafluorobenzenesulphonyl chloride

CAS: 832-53-1

Pentafluorobenzenesulphonyl chloride

Formula: C₆ClF₅O₂S

Purity: 99%

Color and Shape: yellow liquid

Molecular weight: 266.57g/mol

Ref: 54-PC5480

Pentafluorobenzenesulfonyl chloride

CAS: 832-53-1

Pentafluorobenzenesulfonyl chloride is a monosodium salt that is used as an inhibitor in the synthesis of pharmaceuticals and other organic chemicals. It has been shown to inhibit human liver cytochrome P450 enzymes by binding to their heme group. Pentafluorobenzenesulfonyl chloride is also an effective reagent for the determination of the proton concentration in aqueous solutions. This compound reacts with hydrochloric acid (HCl) to form pentafluorobenzenesulfonic acid, which can be detected in urine samples at low concentrations. The reaction rate of this compound with HCl is temperature dependent, and its formation rate increases as the temperature decreases. Pentafluorobenzenesulfonyl chloride has also been shown to possess anticancer properties, due to its reactive functional group. Magnetic particles coated with this substance are being developed for use in cancer treatment.

Formula: C₆ClF₅O₂S

Purity: Min. 98 Area-%

Color and Shape: Colorless Clear Liquid

Molecular weight: 266.57 g/mol

Ref: 3D-FP75671