221006-67-3 Usage
Uses
Used in Medicinal Chemistry:
4-BROMO-3-METHYLPHENYLBORONIC ACID is used as a synthetic intermediate for the development of pharmaceutical compounds, leveraging its reactivity in cross-coupling reactions to form diverse molecular structures that can exhibit therapeutic properties.
Used in Material Science:
In the field of material science, 4-BROMO-3-METHYLPHENYLBORONIC ACID is used as a precursor for the synthesis of advanced materials, contributing to the creation of new substances with unique electronic, optical, or mechanical properties.
Used in the Suzuki-Miyaura Cross-Coupling Reaction:
4-BROMO-3-METHYLPHENYLBORONIC ACID is utilized as a key reagent in the Suzuki-Miyaura cross-coupling reaction, a method pivotal for forming carbon-carbon bonds in organic synthesis, thereby facilitating the construction of complex organic molecules with potential applications in various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 221006-67-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,2,1,0,0 and 6 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 221006-67:
(8*2)+(7*2)+(6*1)+(5*0)+(4*0)+(3*6)+(2*6)+(1*7)=73
73 % 10 = 3
So 221006-67-3 is a valid CAS Registry Number.
221006-67-3Relevant academic research and scientific papers
Synthesis of new phenylpyridyl scaffolds using the Garlanding approach
Voisin-Chiret, Anne Sophie,Muraglia, Marilena,Burzicki, Grégory,Perato, Serge,Corbo, Filomena,Sopková-De Oliveira Santos, Jana,Franchini, Carlo,Rault, Sylvain
experimental part, p. 8000 - 8005 (2010/10/21)
One-pot reaction for the synthesis of novel phenylpyridyl derivatives and mixed quater phenylpyridyl compounds is described by using the Garlanding approach. The reactions proceed with moderate to good yields in mild conditions and good reaction times. This work represents a second application of the simplicity and versatility of Garlanding concept for the construction of new phenylpyridyl scaffolds, which can be considered as non-peptidic foldamer α-helix mimetics.
