879291-26-6 Usage
Description
2-Phenylpyridine-4-boronic acid pinacol ester is a boronic acid derivative that plays a significant role in organic synthesis and pharmaceutical research. It is known for its enhanced stability and reactivity due to the pinacol ester functionality, which makes it a valuable reagent for cross-coupling reactions and the formation of carbon-carbon bonds. Its versatile reactivity and the capability to introduce functional groups into complex molecular structures have positioned it as a promising building block for the development of pharmaceuticals and agrochemicals.
Uses
Used in Organic Synthesis:
2-Phenylpyridine-4-boronic acid pinacol ester is used as a reagent for cross-coupling reactions, facilitating the functionalization of aromatic compounds. Its pinacol ester group enhances the stability and reactivity of the compound, making it suitable for the formation of carbon-carbon bonds in organic synthesis.
Used in Pharmaceutical Research:
In the pharmaceutical industry, 2-Phenylpyridine-4-boronic acid pinacol ester is used as a building block for the development of new drugs. Its versatile reactivity allows for the introduction of functional groups into complex molecular structures, contributing to the design and synthesis of novel pharmaceutical compounds.
Used in Agrochemical Development:
Similarly, in the agrochemical sector, 2-Phenylpyridine-4-boronic acid pinacol ester is utilized as a key intermediate for the synthesis of agrochemicals. Its ability to form carbon-carbon bonds and introduce functional groups into molecular structures aids in the development of new agrochemicals with improved properties and efficacy.
Check Digit Verification of cas no
The CAS Registry Mumber 879291-26-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,7,9,2,9 and 1 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 879291-26:
(8*8)+(7*7)+(6*9)+(5*2)+(4*9)+(3*1)+(2*2)+(1*6)=226
226 % 10 = 6
So 879291-26-6 is a valid CAS Registry Number.
879291-26-6Relevant articles and documents
Ir-catalyzed borylation of C-H bonds in N-containing heterocycles: Regioselectivity in the synthesis of heteroaryl boronate esters
Mkhalid, Ibraheem A. I.,Coventry, David N.,Albesa-Jove, David,Batsanov, Andrei S.,Howard, Judith A. K.,Perutz, Robin N.,Marder, Todd B.
, p. 489 - 491 (2006)
(Chemical Equation Presented) Blocking the way: Substitution at the 2-position in pyridines and other N-heterocycles blocks N-coordination to an Ir center. This steric hindrance provides a substrate-design criterion that allows the Ir-catalyzed borylation
Cyclo-aryl iridium compound and organic electroluminescence device using the compound
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Paragraph 0056; 0066; 0067; 0068, (2018/04/03)
The present invention discloses a cyclo-aryl iridium compound and a phosphorescent organic electroluminescence (organic EL) device using the cyclo-aryl iridium compound as a light-emitting dopant of the light-emitting layer. The organic EL device has good
METAL COMPLEX AND ORGANIC LIGHT-EMITTING DEVICE
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, (2017/01/09)
A metal complex of formula (I): M(L1)x(L2)y (I) wherein: M is a second or third row transition metal; L1 in each occurrence is independently a light-emitting ligand; L2 is an auxiliary ligand; x is at least 1; y
