2,3-Difluorobenzyl Bromide: A Key Building Block for Fluorinated Compound Synthesis
The introduction of fluorine atoms into organic molecules is a widely adopted strategy in medicinal chemistry and agrochemical research to enhance properties such as metabolic stability, lipophilicity, and binding affinity. Among the versatile reagents enabling this, 2,3-Difluorobenzyl bromide stands out as a critical building block. As a leading manufacturer of fine chemical intermediates, we are committed to providing researchers and formulators with high-quality materials like 2,3-Difluorobenzyl bromide to facilitate their innovative work.
The Significance of Fluorine in Modern Chemistry
Fluorine, due to its unique electronegativity and small atomic size, can profoundly influence the physical and biological characteristics of organic compounds. This has led to a surge in the development of fluorinated pharmaceuticals and agrochemicals, where fluorine substitution often results in improved efficacy, bioavailability, and resistance to metabolic degradation.
2,3-Difluorobenzyl Bromide: Structure and Reactivity
2,3-Difluorobenzyl bromide, with its characteristic C7H5BrF2 molecular formula and CAS number 113211-94-2, is a benzyl bromide derivative featuring two fluorine atoms on the aromatic ring. This specific substitution pattern imparts unique electronic and steric properties. The bromine atom on the benzyl carbon acts as a good leaving group, making the compound highly reactive in nucleophilic substitution reactions. This reactivity allows chemists to readily attach the 2,3-difluorobenzyl moiety to various substrates, incorporating the beneficial effects of fluorine into target molecules.
Applications in Synthesis
The utility of 2,3-Difluorobenzyl bromide as a synthetic intermediate is extensive:
- Pharmaceutical Drug Discovery: It's used to synthesize drug candidates where the difluorobenzyl group is a core structural element, often improving pharmacokinetic profiles. Researchers frequently seek to buy this compound for its role in creating molecules with targeted biological activity.
- Agrochemical Innovation: In crop protection, fluorinated compounds can exhibit enhanced pest control or plant growth regulation properties. Using 2,3-Difluorobenzyl bromide allows for the precise introduction of fluorine to fine-tune these applications.
- Material Science: While less common, the introduction of fluorinated benzyl groups can modify the properties of polymers and specialty materials, imparting characteristics like increased thermal stability or reduced surface energy.
As a manufacturer, we ensure that our 2,3-Difluorobenzyl bromide meets stringent purity standards, typically above 98% or 99%. This high purity is essential for researchers who need reliable results. If you are looking to purchase this crucial building block, consider a supplier with a strong reputation for quality and consistency. We offer this intermediate at competitive prices, making it accessible for your research and development projects. Explore our offerings and secure a dependable source for your synthetic needs.
Perspectives & Insights
Bio Analyst 88
“The Significance of Fluorine in Modern Chemistry Fluorine, due to its unique electronegativity and small atomic size, can profoundly influence the physical and biological characteristics of organic compounds.”
Nano Seeker Pro
“This has led to a surge in the development of fluorinated pharmaceuticals and agrochemicals, where fluorine substitution often results in improved efficacy, bioavailability, and resistance to metabolic degradation.”
Data Reader 7
“2,3-Difluorobenzyl Bromide: Structure and Reactivity 2,3-Difluorobenzyl bromide, with its characteristic C7H5BrF2 molecular formula and CAS number 113211-94-2, is a benzyl bromide derivative featuring two fluorine atoms on the aromatic ring.”