383-28-8

Basic information

• Product Name: 1-BroMo-4-((4-fluorophenyl)sulfonyl)benzene
• Synonyms: 1-BroMo-4-((4-fluorophenyl)sulfonyl)benzene;1-(4-bromophenyl)sulfonyl-4-fluorobenzene
• CAS NO: 383-28-8
• Molecular Formula: C₁₂H₈BrFO₂S
• Molecular Weight: 315.1581232
• Mol File: 383-28-8.mol
• Article Data: 10

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 1-BroMo-4-((4-fluorophenyl)sulfonyl)benzene(CAS DataBase Reference)
• NIST Chemistry Reference: 1-BroMo-4-((4-fluorophenyl)sulfonyl)benzene(383-28-8)
• EPA Substance Registry System: 1-BroMo-4-((4-fluorophenyl)sulfonyl)benzene(383-28-8)

Safety Data

• Hazardous Substances Data: 383-28-8(Hazardous Substances Data)

Usage

General Description

1-Bromo-4-((4-fluorophenyl)sulfonyl)benzene is a chemical compound with the molecular formula C12H8BrFO2S. It is a benzene derivative with a bromine atom attached to the 1-position carbon and a sulfonyl group attached to the 4-position carbon, which in turn is connected to a phenyl ring substituted with a fluorine atom. 1-BroMo-4-((4-fluorophenyl)sulfonyl)benzene is commonly used in organic synthesis and medicinal chemistry as a building block for creating other complex molecules. It may also have potential applications in pharmaceuticals and agrochemicals. Additionally, it is important to handle this compound with caution, as it is potentially harmful if ingested or inhaled and can cause skin and eye irritation upon contact.

Upstream product

• 108-86-1 bromobenzene 
• 349-88-2 4-Fluorobenzenesulfonyl chloride 
• 462-06-6 fluorobenzene 
• 106-53-6 para-bromobenzenethiol 
• 352-34-1 4-fluoro-1-iodobenzene 
• 30427-78-2 (4-bromophenyl)(4-fluorophenyl)sulfane 
• 98-58-8 4-bromobenzenesulfonyl chloride 
• 824-80-6 sodium 4-fluorobenzenesulfinate 
• 106-40-1 4-bromo-aniline 

Downstream Products

• 312-28-7 (4-bromo-3-nitro-phenyl)-(4-fluoro-3-nitro-phenyl)-sulfone 

Relevant articles and documents

Stimuli-responsive cyclometalated platinum complex bearing bent molecular geometry for highly efficient solution-processable OLEDs

Smart materials, such as stimuli-responsive luminescence, have attracted much attentions due to their potential application in semiconductor filed. In this context, platinum complexes of (dfppy-DC)Pt(acac) and (dfppy-O-DC)Pt(acac) were prepared and charac

Synthesis method and application of diphenyl sulfone-based double-chromophore thermally activated delayed fluorescent materials

The invention discloses thermally activated delayed fluorescent materials containing double chromophores, and an application thereof in solution-processible organic electroluminescent devices. A carbazole-diphenyl sulfone blue light-emitting chromophore used as a terminal group and a triphenylamine-anthraquinone orange red light-emitting chromophore used as a central core are connected in non-conjugated and conjugated manners to construct the double-chromophore thermally activated delayed fluorescent materials. The materials are beneficial for separating the spatial distribution of the highestoccupied orbits and the lowest empty orbits of molecules to obtain a small energy gap between a single state and a triple state; and the intramolecular energy transfer of the materials changes with the connection mode, and dual emission of the single molecules is achieved. The double-chromophore thermally activated delayed fluorescent materials can be used as the luminescent layer material of a solution-processible organic electroluminescent diode to make the devices have a maximum external quantum efficiency of 3.96%.

Optimized trade-offs between triplet emission and transparency in Pt(II) acetylides through phenylsulfonyl units for achieving good optical power limiting performance

Three Pt(ii) acetylides have been prepared by coupling trans-[PtCl2(PBu3)2] to ethynyl aromatic ligands with electron-withdrawing phenylsulfonyl units in high yields (>85%). The investigation of their photophysical behavior has shown that the unique conjugation-breaking configuration of the -SO2- linker in the phenylsulfonyl units can afford a very short cut-off wavelength (λcut-off) of P) of the prepared Pt(ii) acetylides can be effectively enhanced from 0.52% to 15.92% through increasing the number of fluorine substituents on the phenylsulfonyl units in the organic ligands. Benefiting from their enhanced ΦP, the phenylsulfonyl-based Pt(ii) acetylides can exhibit comparable or even better optical power limiting (OPL) performance against 532 nm lasers than the state-of-the-art OPL material C60, indicating their great potential in the field of laser protection. All of these results have provided a new strategy to achieve consistency between high OPL ability and good transparency for OPL materials, representing a valuable attempt for coping with key problems in the field of nonlinear optics.