709022-63-9 Usage
Uses
Used in Chemical Synthesis:
9-Anthraceneboronic acid piacol ester is used as a reactant for the synthesis of a series of luminescent compounds. Its unique chemical structure allows it to participate in various chemical reactions, leading to the formation of new compounds with potential applications in different industries.
Used in the Pharmaceutical Industry:
In the pharmaceutical industry, 9-Anthraceneboronic acid piacol ester is used as a building block for the development of novel drugs. Its reactivity and structural features make it a valuable component in the design and synthesis of new drug candidates, particularly those with potential applications in the treatment of various diseases.
Used in the Material Science Industry:
9-Anthraceneboronic acid piacol ester is also used in the material science industry for the development of new materials with specific optical and electronic properties. The luminescent compounds synthesized using this intermediate can be utilized in the creation of advanced materials for applications such as light-emitting diodes (LEDs), sensors, and other optoelectronic devices.
Used in the Research and Development Sector:
In the research and development sector, 9-Anthraceneboronic acid piacol ester serves as an important tool for scientists and researchers working on the development of new chemical compounds and materials. Its unique properties and reactivity make it a valuable asset in the exploration of new chemical reactions and the synthesis of novel compounds with potential applications in various fields.
Check Digit Verification of cas no
The CAS Registry Mumber 709022-63-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,0,9,0,2 and 2 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 709022-63:
(8*7)+(7*0)+(6*9)+(5*0)+(4*2)+(3*2)+(2*6)+(1*3)=139
139 % 10 = 9
So 709022-63-9 is a valid CAS Registry Number.
709022-63-9Relevant academic research and scientific papers
Wa?e?sa-Chorab, Monika,Kubicki, Maciej,Patroniak, Violetta
, p. 805 - 809 (2014)
New bianthracene-quaterpyridine ligand 6,6″′-bis(anthracen-9- yl)-2,2′;6′,2″;6″,2″′-quaterpyridine L has been obtained in a multistep synthesis using Suzuki-Miyaura and Stille-type coupling reactions. The dianthracene ligand L has four nitrogen-donor atoms and can form different supramolecular architectures with transition metal ions. Ligand L and intermediate compounds have been characterized by spectroscopic methods and elemental analyses. 2-(Anthracen-9-yl)-6-bromopyridine and 6-(anthracen-9-yl)-6′-bromo-2,2′-bipyridine have been also characterized by X-ray crystallography.
Application of cooperative iron/copper catalysis to a palladium-free borylation of aryl bromides with pinacolborane
Labre, Flavien,Gimbert, Yves,Bannwarth, Pierre,Olivero, Sandra,Dunach, Elisabet,Chavant, Pierre Y.
supporting information, p. 2366 - 2369 (2014/05/20)
A new cooperative copper/iron catalysis for the borylation of various aryl bromides with pinacolborane, at -10 °C, is reported. Use of the toxic, precious metal Pd is avoided. The mechanism of the protodebromination side reaction is discussed.
