778-36-9

Basic information

• Product Name: PENTAFLUOROBENZENESULPHONAMIDE
• Synonyms: PENTAFLUOROBENZENESULPHONAMIDE;PENTAFLUORBENZENESULFONAMIDE
• CAS NO: 778-36-9
• Molecular Formula: C₆H₂F₅NO₂S
• Molecular Weight: 247.14
• Mol File: 778-36-9.mol
• Article Data: 8

Chemical Properties

• Melting Point: 155-156 °C
• Boiling Point: 292.4±50.0 °C(Predicted)
• Appearance: /
• Density: 1.772±0.06 g/cm3(Predicted)
• PKA: 8.80±0.60(Predicted)
• CAS DataBase Reference: PENTAFLUOROBENZENESULPHONAMIDE(CAS DataBase Reference)
• NIST Chemistry Reference: PENTAFLUOROBENZENESULPHONAMIDE(778-36-9)
• EPA Substance Registry System: PENTAFLUOROBENZENESULPHONAMIDE(778-36-9)

Safety Data

• Hazard Codes: Xi
• Hazardous Substances Data: 778-36-9(Hazardous Substances Data)

Usage

General Description

Pentafluorobenzenesulphonamide is a chemical compound with the molecular formula C6H4F5NO2S. It is a white powder that is used as a precursor in organic synthesis, particularly in the production of pharmaceuticals, agrochemicals, and materials science. Pentafluorobenzenesulphonamide exhibits strong electron-withdrawing properties due to the presence of the sulphonamide and pentafluorobenzene functional groups, making it a useful reagent in a variety of chemical reactions. Additionally, it is known for its high thermal stability and inertness, making it a valuable component in the development of new materials for various industrial applications. However, it is important to handle and store pentafluorobenzenesulphonamide with care, as it can be hazardous if not used properly.

Upstream product

• 1313-13-9 manganese(IV) oxide 
• 54556-76-2 pentafluorobenzenesulfinamide 
• 832-53-1 pentafluorobenzenesulonyl chloride 
• 31377-92-1 pentafluorophenylmercaptoamine 
• 36649-97-5 pentafluorobenzenesulfinyl chloride 
• 863033-38-9 Acetic acid (2R,3R,4R,5R)-4-acetoxy-5-acetoxymethyl-2-(6-oxo-1-pentafluorobenzenesulfonyl-1,6-dihydro-purin-9-yl)-tetrahydro-furan-3-yl ester 
• 58749-38-5 N,N-dichloropentafluoroaniline 
• 73750-52-4 Se,Se-dichloro-N-pentafluorophenylsulphonylselenoimine 

Downstream Products

• 4400-88-8 2,3,5,6-Tetrafluoro-4-(2-hydroxy-ethylamino)-benzenesulfonamide 
• 17140-77-1 2-amino-ethanol; hydro fluoride 
• 7074-89-7 CH₂CH₂CH₂CH₂NC₆F₄SO₂NH₂ 
• 51587-32-7 pentafluorophenylsulfonylisocyanate 
• 62726-36-7 iPrNH₂*HF 
• 4365-24-6 2,3,5,6-Tetrafluoro-4-isopropylamino-benzenesulfonamide 
• 4365-19-9 4-Cyclopentylamino-2,3,5,6-tetrafluoro-benzenesulfonamide 
• 4408-99-5 4-Cyclohexylamino-2,3,5,6-tetrafluoro-benzenesulfonamide 
• 26593-77-1 cyclohexylamine hydrofluoride 
• 1613266-96-8 2,3,5,6-tetrafluoro-4-(4-p-tolyl-1H-1,2,3-triazol-1-yl)benzenesulfonamide 
• 1613266-97-9 2,3,5,6-tetrafluoro-4-(4-phenyl-1H-1,2,3-triazol-1-yl)benzenesulfonamide 
• 1613266-86-6 4-(4-(cyclohexylmethyl)-1H-1,2,3-triazol-1-yl)-2,3,5,6 tetrafluorobenzenesulfonamide 
• 1613266-98-0 2,3,5,6-tetrafluoro-4-(4-(4-pentylphenyl)-1H-1,2,3-triazol-1-yl)benzenesulfonamide 
• 1613266-99-1 4-(4-(2-bromoethyl)-1H-1,2,3-triazol-1-yl)-2,3,5,6-tetrafluorobenzenesulfonamide 

Relevant articles and documents

FBSA-BASED THERAPEUTIC AND RADIOIMAGING CONJUGATES TARGETING CARBONIC ANHYDRASE POSITIVE CANCERS

The present disclosure relates to compositions and methods of carbonic anhydrase IX inhibitors. The present disclosure also relates to targeting conjugates of carbonic anhydrase IX inhibitors. The present disclosure also relates to the use of targeting co

COLORING COMPOSITION, CURED FILM, COLOR FILTER, MANUFACTURING METHOD FOR COLOR FILTER, SOLID STATE IMAGING ELEMENT, AND IMAGE DISPLAY DEVICE

PROBLEM TO BE SOLVED: To provide a coloring composition with which it is possible to solve planar irregularities, and a cured film, a color filter, a method for producing a color filter, a solid state imaging element, and an image display device using the coloring composition. SOLUTION: A coloring composition contains a pigment compound represented by the left formula, a curable compound, and a solvent, the pigment compound represented by the left formula having a counter anion inside and/or outside the molecule, wherein one of Ar1 and Ar2 is a group represented by the right formula; the other is a hydrogen atom, a group represented by the right formula, or the like; R5 and R6 independently represent hydrogen atoms or the like; R7 represents a monovalent substituent; R8 represents a halogen atom or the like; p is an integer from 0 to 4; R1 and R2 independently represent alkyl groups having 3 or more carbon atoms or the like; X1 to X3 independently represent hydrogen atoms or the like. COPYRIGHT: (C)2015,JPOandINPIT

4-Substituted-2,3,5,6-tetrafluorobenzenesulfonamides as inhibitors of carbonic anhydrases I, II, VII, XII, and XIII

A series of 4-substituted-2,3,5,6-tetrafluorobenezenesulfonamides were synthesized and their binding potencies as inhibitors of recombinant human carbonic anhydrase isozymes I, II, VII, XII, and XIII were determined by the thermal shift assay, isothermal