1028205-76-6 Usage
Uses
Used in Organic Synthesis:
2,3,4,5,6-Pentamethylphenylboronic acid is used as a building block in organic synthesis for the formation of carbon-carbon and carbon-heteroatom bonds. Its unique properties allow for the creation of complex organic molecules with specific structural features.
Used in Pharmaceutical Development:
In the pharmaceutical industry, 2,3,4,5,6-Pentamethylphenylboronic acid is used as a key intermediate in the synthesis of various drug molecules. Its ability to form stable bonds with other chemical entities makes it a promising candidate for the development of new therapeutic agents.
Used in Agrochemical Production:
Similarly, in the agrochemical sector, 2,3,4,5,6-Pentamethylphenylboronic acid is utilized as a precursor in the synthesis of agrochemicals, such as pesticides and herbicides. Its reactivity and stability contribute to the creation of effective and targeted agrochemical products.
Used in Catalytic Processes:
2,3,4,5,6-Pentamethylphenylboronic acid has also been studied for its potential use in catalytic processes. Its ability to form stable intermediates with transition metals makes it a candidate for use in catalytic reactions, potentially improving the efficiency and selectivity of various chemical transformations.
Used in Organic Transformations:
Furthermore, 2,3,4,5,6-Pentamethylphenylboronic acid is employed in organic transformations, where it can act as a reagent to modify the structure of organic compounds. Its unique properties enable the conversion of one functional group to another, facilitating the synthesis of a wide range of organic compounds.
Check Digit Verification of cas no
The CAS Registry Mumber 1028205-76-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,2,8,2,0 and 5 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1028205-76:
(9*1)+(8*0)+(7*2)+(6*8)+(5*2)+(4*0)+(3*5)+(2*7)+(1*6)=116
116 % 10 = 6
So 1028205-76-6 is a valid CAS Registry Number.
1028205-76-6Relevant academic research and scientific papers
Supramolecular structures and spontaneous resolution: The case of ortho-substituted phenylboronic acids
Filthaus, Matthias,Oppel, Iris M.,Bettinger, Holger F.
scheme or table, p. 1201 - 1207 (2008/10/09)
The solid state structures of a number of ortho-substituted arylboronic acids, ortho-bromophenyl, ortho-phenylphenyl, pentamethylphenyl, and 10-bromo-9-anthryl, were determined by X-ray diffraction techniques. All boronic acids investigated form dimers in the solid state, but the interconnection of dimers to ribbons differs from that of the parent phenylboronic acid. Pentamethylphenylboronic acid only uses one hydrogen bond but an additional OH-π interaction for connection of dimers, while all others investigated employ two hydrogen bonds for interconnection of dimers to ribbons. 10-Bromo-9-anthrylboronic acid is found to undergo spontaneous resolution of its enantiomers to a racemic conglomerate upon crystallization. The Royal Society of Chemistry.
