163517-61-1 Usage
Description
2-Methyl-3-fluoro-phenylboronic acid is a chemical compound with the molecular formula C7H8BFO2. It is predominantly used in pharmaceutical research and development due to its functional boronic acid group. This group is valuable for carbon-carbon bond formation in various types of synthetic reactions, as it can react with organic or inorganic substances. The additional fluorine atom in the compound helps to modify the properties of the final product, such as its reactivity, polarity, and bioavailability.
Uses
Used in Pharmaceutical Research and Development:
2-Methyl-3-fluoro-phenylboronic acid is used as a key intermediate in the synthesis of complex organic substances, particularly in the pharmaceutical industry. Its boronic acid group facilitates carbon-carbon bond formation, making it a versatile building block for the creation of new drug molecules.
Used in the Suzuki Reaction:
2-Methyl-3-fluoro-phenylboronic acid is used as a reactant in the Suzuki reaction, a palladium-catalyzed coupling reaction. This reaction is highly useful in the synthesis of complex organic molecules, including those found in pharmaceutical compounds. The presence of the boronic acid group allows for the formation of carbon-carbon bonds, which are essential for constructing the desired molecular structures.
Used in Modifying Properties of Final Products:
The additional fluorine atom in 2-methyl-3-fluoro-phenylboronic acid is used to modify the properties of the final product, such as its reactivity, polarity, and bioavailability. This modification can be crucial in the development of more effective pharmaceutical compounds, as it can influence the compound's interaction with biological targets and its overall efficacy.
Used in Organic Synthesis:
2-Methyl-3-fluoro-phenylboronic acid is used as a reagent in various organic synthesis reactions. Its boronic acid group can react with a wide range of organic and inorganic substances, making it a valuable tool for the formation of carbon-carbon bonds and the construction of complex molecular structures. This versatility is particularly useful in the development of new pharmaceutical compounds and other organic products.
Check Digit Verification of cas no
The CAS Registry Mumber 163517-61-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,3,5,1 and 7 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 163517-61:
(8*1)+(7*6)+(6*3)+(5*5)+(4*1)+(3*7)+(2*6)+(1*1)=131
131 % 10 = 1
So 163517-61-1 is a valid CAS Registry Number.
InChI:InChI=1/C7H8BFO2/c1-5-6(8(10)11)3-2-4-7(5)9/h2-4,10-11H,1H3
