CAS 6287-38-3: A Deep Dive into 3,4-Dichlorobenzaldehyde Applications
For research scientists, formulation chemists, and product developers, understanding the specific applications of chemical intermediates is vital. 3,4-Dichlorobenzaldehyde, known by its CAS number 6287-38-3, stands out as a versatile compound with significant utility, particularly within the pharmaceutical sector and broader organic synthesis. As a reliable manufacturer and supplier, we aim to provide insights into how this chemical intermediate powers innovation.
The Core Role: Pharmaceutical Synthesis
The most prominent application of 3,4-Dichlorobenzaldehyde is its role as a key intermediate in the synthesis of various pharmaceuticals. Its structure, featuring an aldehyde group and two strategically placed chlorine atoms, makes it an excellent starting material for building complex molecular architectures. A prime example cited in literature is its use in the synthesis of nitroquine, a drug with antimalarial properties. The precise structure of 3,4-Dichlorobenzaldehyde allows chemists to introduce specific functionalities and modifications, leading to the development of life-saving medications.
Beyond Pharmaceuticals: Versatile Organic Synthesis
The utility of 3,4-Dichlorobenzaldehyde extends beyond just pharmaceuticals. As a reactive aldehyde, it can participate in a multitude of organic reactions, including:
- Condensation Reactions: The aldehyde group can readily react with amines, active methylene compounds, and other nucleophiles to form new carbon-carbon or carbon-heteroatom bonds.
- Oxidation and Reduction: It can be oxidized to the corresponding carboxylic acid or reduced to the alcohol, providing pathways to different functional groups.
- Wittig and Grignard Reactions: These reactions allow for the extension of the carbon chain and the introduction of various substituents.
These versatile reaction capabilities make 3,4-Dichlorobenzaldehyde an invaluable component for chemists working on:
- Agrochemicals: As an intermediate in the synthesis of pesticides, herbicides, or plant growth regulators.
- Dyes and Pigments: Its aromatic structure can be incorporated into chromophores for colorants.
- Material Science: Potentially used in the development of specialty polymers or electronic materials where its specific functional groups are advantageous.
- Flavor and Fragrance Compounds: In some niche applications, aromatic aldehydes contribute to specific scent profiles.
Quality and Sourcing
When you intend to buy 3,4-Dichlorobenzaldehyde for these applications, ensuring its quality and consistent availability is paramount. Researchers and formulators often require high purity (e.g., 99%) to guarantee the efficacy and safety of the final product. Sourcing from a reliable manufacturer, especially one based in China known for its chemical production capabilities, ensures that you receive a product that meets stringent specifications, such as a white crystalline appearance and accurate CAS 6287-38-3 identification.
As a dedicated supplier of 3,4-Dichlorobenzaldehyde, we understand the critical nature of these applications. We are committed to providing high-quality intermediates that enable scientific discovery and product development. If your research or production involves the synthesis of pharmaceuticals like nitroquine or other complex organic molecules, inquire about our 3,4-Dichlorobenzaldehyde to secure a dependable supply.
Perspectives & Insights
Core Pioneer 24
“The precise structure of 3,4-Dichlorobenzaldehyde allows chemists to introduce specific functionalities and modifications, leading to the development of life-saving medications.”
Silicon Explorer X
“Beyond Pharmaceuticals: Versatile Organic Synthesis The utility of 3,4-Dichlorobenzaldehyde extends beyond just pharmaceuticals.”
Quantum Catalyst AI
“As a reactive aldehyde, it can participate in a multitude of organic reactions, including: Condensation Reactions: The aldehyde group can readily react with amines, active methylene compounds, and other nucleophiles to form new carbon-carbon or carbon-heteroatom bonds.”