185626-73-7

Basic information

• Product Name: (3-Bromophenyl)triphenylsilane
• Synonyms: (3-Bromophenyl)triphenylsilane;Silane, (3-bromophenyl)triphenyl-;3-bromophenyltriphenylsilyl chloride;1-bromo-3-(triphenylsilyl)-Benzene
• CAS NO: 185626-73-7
• Molecular Formula: C₂₄H₁₉BrSi
• Molecular Weight: 415.39716
• Mol File: 185626-73-7.mol
• Article Data: 9

Chemical Properties

• Melting Point: 135.0 to 139.0 °C
• Boiling Point: 469.9±37.0 °C(Predicted)
• Appearance: /
• Density: 1.30±0.1 g/cm3(Predicted)
• Storage Temp.: Sealed in dry,Room Temperature
• CAS DataBase Reference: (3-Bromophenyl)triphenylsilane(CAS DataBase Reference)
• NIST Chemistry Reference: (3-Bromophenyl)triphenylsilane(185626-73-7)
• EPA Substance Registry System: (3-Bromophenyl)triphenylsilane(185626-73-7)

Safety Data

• Hazardous Substances Data: 185626-73-7(Hazardous Substances Data)

Usage

General Description

(3-Bromophenyl)triphenylsilane is a chemical compound with the molecular formula C24H20BrSi. It is a silane compound that consists of a brominated phenyl group attached to a triphenylsilane moiety. (3-Bromophenyl)triphenylsilane is commonly used as a building block in organic synthesis and is known for its ability to undergo various chemical reactions, including cross-coupling reactions and nucleophilic substitution reactions. (3-Bromophenyl)triphenylsilane is used as a reagent in the preparation of various organic compounds and is also employed in material science research for its unique properties. It is known to be air and moisture sensitive and should be handled with care in a controlled environment.

Upstream product

• 76-86-8 Triphenylsilyl chloride 
• 108-36-1 1,3-dibromobenzene 

Downstream Products

• 1329603-61-3 C₄₄H₃₁N₃SSi 
• 1253912-58-1 B-[3-(triphenylsilyl)phenyl]-boronic acid 
• 1329604-11-6 C₂₈H₂₁ClN₂Si 
• 1391041-75-0 triphenyl [3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]silane 
• 1357066-10-4 C₄₆H₃₁N₃SSi 
• 1253911-56-6 C₄₀H₂₉N₃Si 

Relevant articles and documents

Yellow electrophosphorescent devices with hosts containing N1-(naphthalen-1-yl)-N1,N4-diphenylnaphthalene-1,4-diamine and tetraphenylsilane units

Two novel host materials, N1-(naphthalen-1-yl)-N1,N4-diphenyl-N4-(4-(triphenylsilyl)phenyl) naphthalene-1,4-diamine (SiP) and N1-(naphthalen-1-yl)-N1,N4-diphenyl-N4-(3-(triphenylsilyl) phenyl)naphthalene-1,4-diamine (SiM), were synthesised by incorporating a hole-transporting moiety, N1-(naphthalen-1-yl)-N1,N4-diphenylnaphthalene-1,4-diamine (NPNA2) and typical electron-transporting tetraphenylsilane moiety. SiP and SiM materials exhibit high thermal and morphological stability with a glass transition temperature higher than 110°C and decomposition temperature above 350°C. Using Ir(bt)2(acac) (bis(2-phenylbenzothiozolato-N,C2′)iridium(acetylacetonate)) as an emitter, yellow phosphorescent organic light-emitting diodes of ITO/TAPC (1,1-bis[4-(di-p-tolylamino)phenyl]cyclohexane, 40 nm)/host: Ir(bt)2(acac) (15 wt%, 20 nm)/TmPyPB (1,3,5-tri(m-pyrid-3-yl-phenyl)benzene, 40 nm)/LiF (1 nm)/Al (100 nm) show maximum current and power efficiency of 40.81 cd A-1 and 33.60 lm W-1 with low efficiency roll-off. The current efficiency of 40.10 cd A-1 is still observed at the practically useful brightness value of 1000 cd m-2.

ORGANIC ELECTROLUMINESCENT MATERIALS AND DEVICES

Provided are boron-containing compounds. Also provided are formulations comprising these boron-containing compounds. Further provided are OLEDs and related consumer products that utilize these boron-containing compounds.

New organic electroluminescent compounds and the use of the compound of the organic electroluminescent device

Provided are a novel organic electroluminescent compound and an organic electroluminescent device using the same. When used as a host material of an organic electroluminescent material of an OLED device, the organic electroluminescent compound disclosed herein exhibits good luminous efficiency and excellent life property as compared to the existing host material. Therefore, it may be used to manufacture OLEDs having very superior operation life.