1056475-86-5 Usage
Uses
Used in Organic Synthesis:
3,5-DIMETHYL-4-CHLOROPHENYLBORONIC ACID is used as a reagent in organic synthesis for its ability to facilitate Suzuki-Miyaura coupling reactions. These reactions are essential for the formation of carbon-carbon bonds, which are crucial in constructing complex organic molecules.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, 3,5-DIMETHYL-4-CHLOROPHENYLBORONIC ACID is utilized as a key intermediate in the synthesis of pharmaceuticals. Its involvement in the formation of carbon-carbon bonds allows for the creation of diverse and complex drug molecules with potential therapeutic applications.
Used in the Synthesis of Agrochemicals:
3,5-DIMETHYL-4-CHLOROPHENYLBORONIC ACID is also employed in the agrochemical industry, where it serves as a building block for the synthesis of various agrochemical compounds. Its role in creating carbon-carbon bonds is vital for the development of effective and targeted agrochemical products.
Used in the Construction of Complex Molecular Structures:
3,5-DIMETHYL-4-CHLOROPHENYLBORONIC ACID is used as a valuable tool in the construction of complex molecular structures. Its ability to participate in Suzuki-Miyaura coupling reactions makes it an indispensable component in the synthesis of intricate organic compounds with diverse applications across various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 1056475-86-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,5,6,4,7 and 5 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1056475-86:
(9*1)+(8*0)+(7*5)+(6*6)+(5*4)+(4*7)+(3*5)+(2*8)+(1*6)=165
165 % 10 = 5
So 1056475-86-5 is a valid CAS Registry Number.
1056475-86-5Relevant academic research and scientific papers
Self-Assembly of Nanometer-Sized Boroxine Cages from Diboronic Acids
Ono, Kosuke,Johmoto, Kohei,Yasuda, Nobuhiro,Uekusa, Hidehiro,Fujii, Shintaro,Kiguchi, Manabu,Iwasawa, Nobuharu
supporting information, p. 7015 - 7018 (2015/06/25)
By use of the reversible trimerization of boronic acids, the series of boroxine cages 3-mer, 6-mer, and 12-mer were constructed from rationally designed diboronic acids whose bond angles between two C-B bonds are 60°, 84°, and 117°, respectively. Boroxine
