627526-50-5 Usage
General Description
4,4,5,5-Tetramethyl-2-(4-methylnaphthalen-1-yl)-1,3,2-dioxaborolane is a chemical compound with a unique molecular structure that consists of four methyl groups, a methylnaphthalene moiety, and a dioxaborolane ring. 4,4,5,5-Tetramethyl-2-(4-methylnaphthalen-1-yl)-1,3,2-dioxaborolane is primarily used as a reagent in organic synthesis and chemical reactions, particularly in the formation of carbon-carbon and carbon-heteroatom bonds. It is also a versatile building block in the production of pharmaceuticals, agrochemicals, and materials science. Due to its diverse applications, 4,4,5,5-Tetramethyl-2-(4-methylnaphthalen-1-yl)-1,3,2-dioxaborolane is of interest to researchers and chemical manufacturers for its potential in facilitating the synthesis of complex molecules and materials.
Check Digit Verification of cas no
The CAS Registry Mumber 627526-50-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,2,7,5,2 and 6 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 627526-50:
(8*6)+(7*2)+(6*7)+(5*5)+(4*2)+(3*6)+(2*5)+(1*0)=165
165 % 10 = 5
So 627526-50-5 is a valid CAS Registry Number.
627526-50-5Relevant articles and documents
Potential solution processible phosphorescent iridium complexes toward applications in doped light-emitting diodes: Rapid syntheses and optical and morphological characterizations
Sun, Yi-Heng,Zhu, Xu-Hui,Chen, Zhao,Zhang, Yong,Cao, Yong
, p. 6281 - 6284 (2006)
A series of carbazol-9-yl end-capped red-emitting heteroleptic iridium complexes was readily synthesized using post Suzuki coupling. The appealing solubility, photoluminescent characteristics, and morphological stability enabled the current heteroleptic i
An opportunity for Mg-catalyzed grignard-type reactions: Direct coupling of benzylic halides with pinacolborane with 10 mol % of magnesium
Pintaric, Christine,Olivero, Sandra,Gimbert, Yves,Chavant, Pierre Y.,Dunach, Elisabet
supporting information; experimental part, p. 11825 - 11827 (2010/11/02)
Mg in catalytic amounts as the only metal permits the reductive coupling between benzyl halides and pinacolborane. HBpin acts both as an electrophile and as a reducing agent to regenerate an organomagnesium species in situ. An hydride oxidation mechanism is proposed on the basis of DFT calculations.