1072952-14-7 Usage
Description
2-Amino-4,5-difluorophenylboronic acid is a chemical compound with the molecular formula C6H6BF2NO2. It is a boronic acid derivative that contains an amino group and two fluorine atoms attached to a phenyl ring. 2-AMINO-4,5-DIFLUOROPHENYLBORONIC ACID is known for its versatility in organic synthesis and its ability to participate in Suzuki-Miyaura cross-coupling reactions, making it a valuable reagent for constructing biaryl compounds.
Uses
Used in Organic Synthesis:
2-Amino-4,5-difluorophenylboronic acid is used as a reagent for forming carbon-carbon and carbon-heteroatom bonds in organic synthesis. Its unique structure allows for the creation of a wide range of complex molecules, making it a valuable tool in the development of new chemical compounds.
Used in Pharmaceutical Compounds:
2-Amino-4,5-difluorophenylboronic acid is used as a key intermediate in the preparation of pharmaceutical compounds. Its ability to form stable bonds with other molecules makes it an essential component in the synthesis of various drugs, contributing to the development of new treatments and therapies.
Used in Agrochemicals:
In the agrochemical industry, 2-Amino-4,5-difluorophenylboronic acid is used as a building block for the synthesis of various agrochemical products. Its role in creating stable and effective compounds makes it a crucial component in the development of new pesticides, herbicides, and other agricultural chemicals.
Used in Materials Science Applications:
2-Amino-4,5-difluorophenylboronic acid is used in materials science for the development of new materials with unique properties. Its ability to form strong bonds with other molecules allows for the creation of advanced materials with potential applications in various industries, such as electronics, energy, and biotechnology.
Used in Suzuki-Miyaura Cross-Coupling Reactions:
2-Amino-4,5-difluorophenylboronic acid is used as a reactant in Suzuki-Miyaura cross-coupling reactions, a powerful method for constructing biaryl compounds. This reaction is widely employed in the synthesis of complex organic molecules, including those found in pharmaceuticals, agrochemicals, and materials science. The use of this boronic acid derivative in these reactions contributes to the efficient and selective formation of biaryl compounds, which are important in various applications.
Check Digit Verification of cas no
The CAS Registry Mumber 1072952-14-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,7,2,9,5 and 2 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1072952-14:
(9*1)+(8*0)+(7*7)+(6*2)+(5*9)+(4*5)+(3*2)+(2*1)+(1*4)=147
147 % 10 = 7
So 1072952-14-7 is a valid CAS Registry Number.
