2-Hydroxy-N-(5-nitro-2-thiazolyl)-benzamide

Introducing 2-Hydroxy-N-(5-nitro-2-thiazolyl)-benzamide, a versatile and highly pure chemical compound that holds immense potential for researchers and scientists across various fields. With its unique molecular structure and exceptional quality, this Halogenated Thiazole derivative is poised to unlock new frontiers in pharmaceutical development, agrochemical innovation, and beyond.

At the heart of this compound lies a captivating blend of chemical properties, meticulously crafted to serve the needs of the modern scientific landscape. With a CAS number of 173903-47-4 and a molecular weight of 265.239990234375, 2-Hydroxy-N-(5-nitro-2-thiazolyl)-benzamide presents itself as a solid with a distinct color, offering a reliable and consistent starting point for your research endeavors.

The compound's purity, measured at an impressive 90.0%, ensures that you can trust its performance and rely on the integrity of your experimental results. Its InChIKey, FDTZUTSGGSRHQF-UHFFFAOYSA-N, provides a unique identifier that allows for seamless integration into your research workflows and data management systems.

Unlocking the Potential

The versatility of 2-Hydroxy-N-(5-nitro-2-thiazolyl)-benzamide lies in its diverse applications, catering to the needs of researchers and innovators across multiple disciplines.

Pharmaceutical Research: This compound serves as a valuable building block in the synthesis of novel pharmaceutical compounds. Its unique chemical structure and properties enable the development of innovative drug candidates targeting a wide range of health conditions, from neurological disorders to metabolic diseases. By leveraging the power of 2-Hydroxy-N-(5-nitro-2-thiazolyl)-benzamide, researchers can push the boundaries of pharmaceutical innovation and bring new hope to patients in need.

Agrochemical Development: In the realm of agrochemicals, 2-Hydroxy-N-(5-nitro-2-thiazolyl)-benzamide finds its niche as a key component in the synthesis of advanced crop protection agents. Its distinct molecular structure contributes to the formulation of potent and selective pesticides, helping to safeguard crops, increase yields, and promote sustainable agricultural practices.

Chemical Synthesis: Beyond its pharmaceutical and agrochemical applications, this compound serves as a versatile tool for chemists and material scientists. Its unique properties can be harnessed to create novel materials and compounds with tailored characteristics, such as improved stability, reactivity, or selectivity. The possibilities are endless as researchers explore the untapped potential of 2-Hydroxy-N-(5-nitro-2-thiazolyl)-benzamide in their quest for groundbreaking discoveries.

Safety and Handling

While 2-Hydroxy-N-(5-nitro-2-thiazolyl)-benzamide is a powerful chemical compound, it is essential to handle it with the utmost care and diligence. The compound is classified under hazard class 14.1.5, with specific hazard statements (H315, H319, H335) and precautionary statements (P261, P264, P271, P280, and more) that must be strictly followed.

To ensure the safety of both the researcher and the integrity of the compound, it is crucial to wear appropriate personal protective equipment (PPE), such as protective gloves, clothing, eye protection, and a face mask. Additionally, work in a well-ventilated area or outdoors to minimize the risk of exposure. In the event of skin irritation, eye irritation, or any other adverse effects, seek immediate medical attention.

For optimal storage and long-term preservation of 2-Hydroxy-N-(5-nitro-2-thiazolyl)-benzamide, keep the compound in a cool, well-ventilated environment, with the container tightly closed. Proper storage conditions are essential to maintain the compound's purity and stability, ensuring reliable results in your