1392512-54-7 Usage
Uses
Used in Organic Synthesis:
2,6-Dimethyl-4-fluorophenylboronic acid is used as a reagent in organic synthesis for the formation of carbon-carbon and carbon-heteroatom bonds. Its boronic acid functional group allows it to participate in various reactions, making it a valuable component in the synthesis of complex organic molecules.
Used in Suzuki-Miyaura Cross-Coupling Reactions:
In the field of organic chemistry, 2,6-Dimethyl-4-fluorophenylboronic acid is used as a coupling partner in Suzuki-Miyaura cross-coupling reactions. This reaction is a powerful method for forming biaryl compounds, which are important structural motifs in pharmaceuticals, agrochemicals, and materials science. The use of this boronic acid derivative in such reactions contributes to the synthesis of diverse biaryl compounds with potential applications.
Used in Pharmaceutical and Agrochemical Development:
2,6-Dimethyl-4-fluorophenylboronic acid has been studied for its potential applications in the development of pharmaceuticals and agrochemicals. Its unique structure and reactivity make it a promising candidate for the synthesis of novel bioactive compounds with potential therapeutic or pesticidal properties. Researchers are exploring its use in the design and synthesis of new drug candidates and agrochemicals to address various health and agricultural challenges.
Check Digit Verification of cas no
The CAS Registry Mumber 1392512-54-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,9,2,5,1 and 2 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1392512-54:
(9*1)+(8*3)+(7*9)+(6*2)+(5*5)+(4*1)+(3*2)+(2*5)+(1*4)=157
157 % 10 = 7
So 1392512-54-7 is a valid CAS Registry Number.
1392512-54-7Relevant articles and documents
ANTAGONISTS OF HUMAN INTEGRIN (ALPHA4)(BETA7)
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Paragraph 0228; 0761; 0762, (2019/10/29)
Disclosed are small molecule antagonists of α4β7 integrin, and methods of using them to treat a number of specific diseases or conditions.
Robust acenaphthoimidazolylidene palladium complexes: Highly efficient catalysts for suzuki-miyaura couplings with sterically hindered substrates
Tu, Tao,Sun, Zheming,Fang, Weiwei,Xu, Mizhi,Zhou, Yunfei
supporting information; experimental part, p. 4250 - 4253 (2012/10/07)
Robust acenaphthoimidazolylidene palladium complexes have been demonstrated as highly efficient and general catalysts for the sterically hindered Suzuki-Miyaura cross-coupling reactions in excellent yields even with low catalyst loadings under mild reaction conditions. The high catalytic activity of these complexes highlights that, besides the "flexible steric bulky" concept, σ-donor properties of the NHC ligands are also crucial to accelerate the transformations.
