The Chemical Reactivity of 2-Chloro-4-hydroxybenzaldehyde for Synthesis
Understanding the chemical reactivity of a compound is crucial for any chemist or formulator. 2-Chloro-4-hydroxybenzaldehyde (CAS: 56962-11-9) is a fascinating molecule that offers a wealth of possibilities in organic synthesis due to its distinct functional groups. As a leading manufacturer and supplier of fine chemicals, we provide insights into why this intermediate is so valuable.
The molecule features an aldehyde group, a hydroxyl group, and a chlorine atom attached to a benzene ring. The aldehyde group is susceptible to nucleophilic addition and oxidation, making it a versatile site for transformations like Wittig reactions or reduction to an alcohol. The hydroxyl group, being phenolic, exhibits weak acidity and can participate in etherification or esterification reactions. The presence of the chlorine atom can influence regioselectivity in further aromatic substitution reactions or serve as a leaving group in certain coupling reactions.
This unique combination of functional groups makes 2-Chloro-4-hydroxybenzaldehyde an excellent starting material for constructing more complex molecular architectures. Researchers often look to buy such intermediates from reliable sources to ensure predictable reactivity and yield. We offer this compound with guaranteed high purity, providing a solid foundation for your synthetic endeavors.
Our role as a manufacturer in China means we can offer this chemical at a competitive price, facilitating its widespread use in both academic research and industrial production. Whether your project involves creating novel pharmaceuticals, specialized agrochemicals, or advanced materials, the reactivity profile of 2-Chloro-4-hydroxybenzaldehyde makes it a key ingredient.
We encourage potential buyers to explore the synthetic pathways where this compound can be applied. Feel free to request a quote from our dedicated supplier team. Let us help you unlock the full potential of 2-Chloro-4-hydroxybenzaldehyde in your chemical synthesis projects.
Perspectives & Insights
Future Origin 2025
“The hydroxyl group, being phenolic, exhibits weak acidity and can participate in etherification or esterification reactions.”
Core Analyst 01
“The presence of the chlorine atom can influence regioselectivity in further aromatic substitution reactions or serve as a leaving group in certain coupling reactions.”
Silicon Seeker One
“This unique combination of functional groups makes 2-Chloro-4-hydroxybenzaldehyde an excellent starting material for constructing more complex molecular architectures.”