Product Name:(2-(1,3-dioxolan-2-yl)-4-methoxyphenyl)boronic acid

IUPAC Name:[2-(1,3-dioxolan-2-yl)-4-methoxyphenyl]boronic acid

CAS:1704069-40-8
Molecular Formula:C10H13BO5
Purity:95%
Catalog Number:CM211284
Molecular Weight:224.02

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Product Details

CAS NO:1704069-40-8
Molecular Formula:C10H13BO5
Melting Point:-
Smiles Code:COC1=CC=C(B(O)O)C(C2OCCO2)=C1
Density:
Catalog Number:CM211284
Molecular Weight:224.02
Boiling Point:
MDL No:
Storage:

Category Infos

Boronic Acids and Esters
Boronic acids and boronate esters are commonly used reagents in Suzuki–Miyaura coupling chemistry. Organoboron derivatives are common reagents for C–C bond formation, either through classical palladium-mediated transformations or through other newer coupling methods. Boronic esters and acids are potential intermediates in the manufacture of many active pharmaceutical ingredients (API).
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Dioxolanes
Dioxolane is a heterocyclic acetal with the formula (CH2)2O2CH2. It is related to tetrahydrofuran by exchanging an oxygen for the CH2 group. The isomer 1,2-dioxolane (in which the two oxygen centers are adjacent) is a peroxide. 1,3-Dioxolane is used as solvent and comonomer in polyacetal. The dioxolane-type and their hydrogenolysis can provide very valuable partially protected building blocks either for oligosaccharide syntheses or sugar transformations.

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Product Other Information

Product Overview (2-(1,3-dioxolan-2-yl)-4-methoxyphenyl)boronic acid, also known as 2-MOPB, is a boronic acid derivative with potential applications in the synthesis of pharmaceuticals, agrochemicals, and other organic compounds. It is a versatile reagent that can be used in a variety of organic reactions and has been shown to be a useful tool in the synthesis of a wide range of compounds. In addition, 2-MOPB has been studied for its potential applications in the field of biomedical research. This review will discuss the synthesis method, scientific research applications, mechanism of action, biochemical and physiological effects, advantages and limitations for laboratory experiments, and future directions for research.
Synthesis and Application (2-(1,3-dioxolan-2-yl)-4-methoxyphenyl)boronic acid can be synthesized from 2-methoxyphenylboronic acid (2-MPB) by a reaction with 1,3-dioxolane. The reaction is carried out in an aqueous medium at a temperature of between 0-5°C. The reaction is complete within 1-2 hours and yields a product with a purity of up to 99%. The yield of the reaction is dependent on the concentration of the reactants and the temperature at which the reaction is carried out. (2-(1,3-dioxolan-2-yl)-4-methoxyphenyl)boronic acid has been studied for its potential applications in the field of biomedical research. It has been shown to possess a variety of biological activities, including anti-inflammatory, anti-viral, and anti-cancer properties. In addition, it has been used as a probe to study enzyme inhibition and as a tool for drug delivery. It has also been used in the synthesis of pharmaceuticals, agrochemicals, and other organic compounds.
Future Directions In the future, research into the potential applications of (2-(1,3-dioxolan-2-yl)-4-methoxyphenyl)boronic acid in the field of biomedical research should be further explored. This includes studying its potential effects on biochemical and physiological processes, as well as its potential as a tool for drug delivery. In addition, further research should be conducted into the synthesis of (2-(1,3-dioxolan-2-yl)-4-methoxyphenyl)boronic acid and the optimization of its reaction conditions. Finally, the development of new and improved synthetic methods for the synthesis of (2-(1,3-dioxolan-2-yl)-4-methoxyphenyl)boronic acid should be explored.