Innovating with 2,6-Dichloroaniline: A Chemical Synthesis Guide
For research and development scientists in the chemical industry, identifying and effectively utilizing versatile intermediates is key to innovation. 2,6-Dichloroaniline (CAS 608-31-1) stands out as a crucial building block, enabling the creation of complex molecules with applications spanning pharmaceuticals, agrochemicals, and beyond. This guide is designed for R&D professionals looking to understand the synthesis potential and procurement of this valuable compound. As a dedicated manufacturer and supplier, we aim to provide the insights needed to effectively integrate 2,6-Dichloroaniline into your research and development pipelines.
The Chemical Versatility of 2,6-Dichloroaniline
2,6-Dichloroaniline, with its distinct structure featuring chlorine atoms flanking an amino group on a benzene ring, offers a rich platform for various chemical transformations. Its properties, including a high purity assay of ≥99.0%, make it an ideal starting material for complex organic synthesis. R&D scientists can leverage its reactivity for a range of reactions, including:
- Diazotization: The amino group can be converted into a diazonium salt, which is a highly reactive intermediate for introducing various functionalities, such as halogens, hydroxyl groups, or cyano groups, onto the aromatic ring.
- Acylation and Alkylation: The nitrogen atom can be readily acylated or alkylated to form amides or secondary/tertiary amines, modifying the compound's properties and opening pathways to different molecular structures.
- Coupling Reactions: It can participate in various cross-coupling reactions, such as Buchwald-Hartwig amination or Suzuki coupling, to form new carbon-nitrogen or carbon-carbon bonds.
These synthetic possibilities are critical for developing new APIs, novel agrochemicals, and advanced materials.
Applications Driving R&D with 2,6-Dichloroaniline
The primary applications that drive R&D efforts involving 2,6-Dichloroaniline include:
- Pharmaceutical Discovery: As an intermediate for drugs like Clonidine and Lomefloxacin, R&D scientists are continuously exploring its use in synthesizing new drug candidates with improved efficacy or novel therapeutic mechanisms.
- Agrochemical Innovation: The development of next-generation herbicides and fungicides often involves intricate molecular design where 2,6-Dichloroaniline serves as a foundational element, contributing to selective action and environmental safety.
- Material Science: Research into new polymers, dyes, and functional materials may also utilize 2,6-Dichloroaniline for its specific structural and electronic properties.
Sourcing for Research and Development: Partnering with a Manufacturer
For R&D scientists, having a reliable source for high-quality 2,6-Dichloroaniline is crucial. When planning your research, consider the following when looking to buy this intermediate:
- Purity: Ensure the supplier provides a high assay (≥99.0%) to guarantee reliable and reproducible experimental results.
- Availability: Smaller quantities for initial research and larger volumes for scaling up should be readily accessible.
- Technical Data: Access to comprehensive technical data, including safety data sheets (SDS) and Certificates of Analysis (CoA), is vital for safe handling and experimental planning.
- Supplier Reliability: Partnering with a direct manufacturer ensures consistent quality and support throughout your research journey. Requesting a quote from a trusted supplier is the first step.
As a leading manufacturer, we are dedicated to supporting innovation in the chemical sector. We provide high-purity 2,6-Dichloroaniline that meets the stringent demands of R&D. By choosing us as your supplier, you ensure access to a critical intermediate that can unlock new possibilities in chemical synthesis and product development. Contact us to discuss your research needs and obtain a quote for 2,6-Dichloroaniline.
Perspectives & Insights
Molecule Vision 7
“The Chemical Versatility of 2,6-Dichloroaniline2,6-Dichloroaniline, with its distinct structure featuring chlorine atoms flanking an amino group on a benzene ring, offers a rich platform for various chemical transformations.”
Alpha Origin 24
“Acylation and Alkylation: The nitrogen atom can be readily acylated or alkylated to form amides or secondary/tertiary amines, modifying the compound's properties and opening pathways to different molecular structures.”
Future Analyst X
“Coupling Reactions: It can participate in various cross-coupling reactions, such as Buchwald-Hartwig amination or Suzuki coupling, to form new carbon-nitrogen or carbon-carbon bonds.”