CAS 2131-55-7: The Advantage of p-Chlorophenyl Isothiocyanate in Synthesis
In the intricate world of chemical synthesis, specific molecular structures unlock unique pathways to desired compounds. p-Chlorophenyl Isothiocyanate, with its CAS number 2131-55-7, is one such molecule that offers significant advantages for researchers and industrial chemists alike. As a trusted manufacturer and supplier, NINGBO INNO PHARMCHEM CO.,LTD. specializes in providing this high-quality intermediate, understanding its crucial role in enabling efficient and effective synthesis processes. For those looking to buy p-Chlorophenyl Isothiocyanate, appreciating its inherent benefits is key to optimizing your R&D and production efforts.
The Chemical Reactivity Driving Innovation
The primary advantage of p-Chlorophenyl Isothiocyanate lies in the inherent reactivity of the isothiocyanate group (-N=C=S). This functional group readily participates in nucleophilic addition reactions with amines, alcohols, and thiols, forming thioureas, thiocarbamates, and dithiocarbamates, respectively. These resulting compounds are foundational for building more complex molecular architectures. The presence of the para-chlorine atom on the phenyl ring further influences the electronic properties of the molecule, often enhancing reactivity or providing a handle for subsequent substitution reactions, thereby expanding the synthetic scope.
Benefits in Pharmaceutical and Agrochemical Synthesis
For the pharmaceutical industry, p-Chlorophenyl Isothiocyanate serves as a vital starting material for synthesizing a range of therapeutic agents. Its derivatives can exhibit antibacterial, antifungal, antiviral, and anticancer activities, making it a valuable intermediate in drug discovery and development. Similarly, in the agrochemical sector, compounds derived from p-Chlorophenyl Isothiocyanate are utilized as pesticides, herbicides, and plant growth regulators, contributing to enhanced crop yields and protection. The ability to reliably purchase high-purity material from a dedicated supplier like us ensures that these critical applications benefit from consistent quality.
Our Manufacturing Excellence for Your Advantage
At NINGBO INNO PHARMCHEM CO.,LTD., our commitment to quality manufacturing means that when you buy p-Chlorophenyl Isothiocyanate, you are acquiring a product with an assay of ≥99.0%. Our established synthesis routes, refined over years of experience, ensure that this intermediate is produced efficiently and with minimal impurities. This focus on quality translates directly into tangible advantages for our clients:
- Reduced Side Reactions: High purity minimizes unwanted side reactions during complex syntheses, leading to cleaner reaction profiles and higher yields of your target molecule.
- Consistent Product Performance: The reliability of our p-Chlorophenyl Isothiocyanate guarantees predictable outcomes in your synthetic procedures, crucial for scale-up and commercial production.
- Cost-Effectiveness: By providing a high-quality intermediate at a competitive price, we help our clients optimize their overall production costs, enhancing their market competitiveness.
Partner with a Trusted Supplier
Choosing the right supplier for essential chemical intermediates like p-Chlorophenyl Isothiocyanate is a strategic decision. We, as a leading manufacturer and supplier based in China, are dedicated to supporting your synthetic endeavors. We invite you to explore the advantages that our high-purity p-Chlorophenyl Isothiocyanate can bring to your projects. Contact us today to learn more about our product specifications, bulk purchase options, and to request a quote. Unlock new possibilities in your research and development with our commitment to excellence.
Perspectives & Insights
Molecule Vision 7
“For those looking to buy p-Chlorophenyl Isothiocyanate, appreciating its inherent benefits is key to optimizing your R&D and production efforts.”
Alpha Origin 24
“The Chemical Reactivity Driving Innovation The primary advantage of p-Chlorophenyl Isothiocyanate lies in the inherent reactivity of the isothiocyanate group (-N=C=S).”
Future Analyst X
“This functional group readily participates in nucleophilic addition reactions with amines, alcohols, and thiols, forming thioureas, thiocarbamates, and dithiocarbamates, respectively.”