850264-92-5 Usage
General Description
3,3'-bis(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1,1'-biphenyl, also known as BMBP, is a chemical compound commonly used in organic electronics and optoelectronic devices due to its high thermal stability and efficient energy transfer properties. It has a unique structure consisting of two boronate ester groups attached to a biphenyl backbone, which allows for effective blue-light emission. BMBP is often employed as a fluorescent dopant in organic light-emitting diodes (OLEDs), where it acts as a host material to improve device performance and longevity. Its outstanding thermal and photophysical properties make BMBP a promising candidate for next-generation display and lighting technologies.
Check Digit Verification of cas no
The CAS Registry Mumber 850264-92-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,5,0,2,6 and 4 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 850264-92:
(8*8)+(7*5)+(6*0)+(5*2)+(4*6)+(3*4)+(2*9)+(1*2)=165
165 % 10 = 5
So 850264-92-5 is a valid CAS Registry Number.
850264-92-5Relevant articles and documents
Fluorescence Enhancement of Aromatic Macrocycles by Lowering Excited Singlet State Energies
Ikemoto, Koki,Tokuhira, Toshiki,Uetani, Akari,Harabuchi, Yu,Sato, Sota,Maeda, Satoshi,Isobe, Hiroyuki
, p. 150 - 157 (2020)
A series of cyclo-meta-phenylene congeners with a variation of interphenylene bridges was synthesized by adopting concise synthetic routes to investigate the structure-fluorescence relationships of macrocycles. With fundamental UV-vis absorption and fluor
Oxidative homocoupling reaction of aryltrimethylsilanes by Pd/o-chloranil catalysis
Shibata, Mari,Ito, Hideto,Itami, Kenichiro
supporting information, p. 1701 - 1704 (2017/11/23)
A practical oxidative homocoupling reaction of aryltri-methylsilanes has been achieved by Pd/o-chloranil catalytic system. The reaction shows the good functional group tolerability toward bromo, fluoro, ester, and methoxy groups to give a series of biaryls bearing electron-withdrawing and -donating groups. The boronate group is also retained on biaryls without any ArB bond cleavage, which is highly advantageous for orthogonal coupling.
