18826-13-6 Usage
Description
4,4'-Bis(triphenylsilyl)-1,1'-biphenyl, also known as BSB, is an organic compound with a unique structure consisting of two triphenyllsilanes connected by a biphenyl spacer. 4,4'-Bis(triphenylsilyl)-1,1'-biphenyl is a member of a family of related compounds, with another example being UGH-2, which features a phenyl spacer instead.
Uses
Used in Chemical Synthesis:
4,4'-Bis(triphenylsilyl)-1,1'-biphenyl is used as a key intermediate in the synthesis of various organic compounds, particularly those involving silicon-containing moieties. Its unique structure allows for the formation of complex molecules with potential applications in materials science and pharmaceuticals.
Used in Materials Science:
In the field of materials science, 4,4'-Bis(triphenylsilyl)-1,1'-biphenyl is utilized as a building block for the development of novel materials with specific properties. Its ability to form stable structures with other molecules makes it a valuable component in the creation of advanced materials with potential applications in electronics, optics, and other high-tech industries.
Used in Pharmaceutical Research:
4,4'-Bis(triphenylsilyl)-1,1'-biphenyl is also used as a starting material in the pharmaceutical industry for the development of new drugs. Its unique structure and reactivity make it a promising candidate for the synthesis of bioactive compounds with potential therapeutic applications.
Used in Research and Development:
Due to its unique structure and properties, 4,4'-Bis(triphenylsilyl)-1,1'-biphenyl is often used in research and development settings to explore new chemical reactions, mechanisms, and applications. Its versatility allows scientists to investigate a wide range of potential uses and develop innovative solutions in various fields.
Check Digit Verification of cas no
The CAS Registry Mumber 18826-13-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,8,2 and 6 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 18826-13:
(7*1)+(6*8)+(5*8)+(4*2)+(3*6)+(2*1)+(1*3)=126
126 % 10 = 6
So 18826-13-6 is a valid CAS Registry Number.
18826-13-6Relevant articles and documents
Arylsilane compound, arylsilane polymer and application thereof
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Page/Page column 0068-0070, (2021/02/10)
The invention relates to an arylsilane compound, an arylsilane polymer and application thereof. The structural formula of the arylsilane compound is shown as a formula I in the specification. The arylsilane compound takes an aryl unit as a core, an aryl s
BIS-TRIPHENYLSILYL COMPOUNDS AND THEIR APPLICATION ON ORGANIC ELECTRONIC DEVICE
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Page/Page column 4, (2009/05/28)
The present invention discloses a bis-triphenylsilyl compound and its applications as a host material, electron transport material, or hole transport material in an organic electronic device. The general structure of the bis-triphenylsilyl compound is as follows: where G represents any atomic moiety or single bond of the functional group selected from the group consisting of the following: aryl group, cyclene group, and heterocyclic ring group; and R1?R32 represent substituents on aryl groups.
A deep red phosphorescent Ir(III) complex for use in polymer light-emitting diodes: Role of the arylsilyl substituents
You, Ngmin,An, Cheng-Guo,Kim, Jang-Joo,Soo, Young Park
, p. 6241 - 6246 (2008/02/09)
(Figure Presented) Here we report the synthesis and electrophosphorescence of a new deep-red phosphorescent Ir(III) complex with spatially embracing and thus solubilizing arylsilyl-substituted ligands, Ir(III) tris(2-(2′- benzo[b]thienyl)-5-(4′-triphenylsilylphenyl)pyridinato-N,C 3′). A poly(N-vinylcarbazole) (PVK) film doped with this Ir(III) complex exhibited excellent phase homogeneity and showed saturated red electrophosphorescence of 2.7% maximum external quantum efficiency, whose Commission Internationale de L'Eclairage coordinates were (0.69, 0.30).
