Methyl cinnoline-6-carboxylate - 250mg

REF #: 10-F220647
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Short description

Methyl cinnoline-6-carboxylate

Discover the exceptional Methyl cinnoline-6-carboxylate, a high-purity (95.0%) chemical compound with a molecular weight of 188.18600463867188. This versatile compound, bearing the CAS number 318276-74-3, offers a unique blend of reactivity and selectivity, making it a valuable asset for your research and development needs. However, handle with care as it is classified as harmful if swallowed, causes skin irritation, and may cause respiratory irritation. Always follow safety protocols and store in a well-ventilated area. Unlock the potential of this premium-quality chemical and elevate your experiments to new heights.

  • CAS: 318276-74-3
  • Purity: 95.0%
  • Molecular Weight: 188.18600463867188
  • InChIKey: JMLKGGQGRGKUFU-UHFFFAOYSA-N
$342
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  • Procurenet Team Tshim Sha Tsui
    Hong Kong Hong Kong 3 years
Description

Methyl cinnoline-6-carboxylate

Methyl cinnoline-6-carboxylate, with the CAS number 318276-74-3, is a highly specialized and purified chemical compound that holds immense potential for researchers and scientists across various fields. This Cinnoline and Impurities derivative boasts a unique molecular structure and a purity level of 95.0%, making it a valuable asset in the pursuit of scientific advancements.

At the heart of this compound lies a cinnoline core, a heterocyclic aromatic system that has garnered significant attention in the scientific community. The addition of a carboxylate group at the sixth position, along with a methyl substituent, imbues Methyl cinnoline-6-carboxylate with distinct chemical properties and reactivity. This combination of structural features opens up a world of possibilities for researchers, allowing them to explore the compound's versatile applications in diverse domains.

Pharmaceutical Research and Development

In the realm of pharmaceutical research, Methyl cinnoline-6-carboxylate serves as a crucial building block in the synthesis of innovative drug candidates. Its unique molecular architecture can be leveraged to develop compounds with improved pharmacological profiles, targeting a wide range of health conditions. Researchers in this field can harness the compound's reactivity and selectivity to create novel therapeutic agents, potentially leading to breakthroughs in the treatment of various diseases.

The cinnoline scaffold, with its inherent biological activity, has long been recognized as a valuable scaffold in medicinal chemistry. By incorporating the Methyl cinnoline-6-carboxylate moiety into their synthetic strategies, pharmaceutical scientists can explore new avenues for drug discovery, unlocking the potential to address unmet medical needs.

Agrochemical Applications

Beyond the pharmaceutical realm, Methyl cinnoline-6-carboxylate also finds applications in the agrochemical industry. Its distinct chemical properties can contribute to the development of advanced crop protection agents, such as pesticides and herbicides. The cinnoline core and the carboxylate functionality can be leveraged to create targeted and selective agrochemical compounds, helping to safeguard crops, enhance yields, and promote sustainable agricultural practices.

The versatility of Methyl cinnoline-6-carboxylate allows agrochemical researchers to explore innovative formulations and delivery systems, ultimately leading to more effective and environmentally-friendly solutions for modern agriculture.

Chemical Synthesis and Material Science

In the broader realm of chemical synthesis, Methyl cinnoline-6-carboxylate serves as a valuable reagent and building block. Its unique structural features and reactivity patterns enable chemists to explore the creation of novel compounds with tailored properties. These compounds may find applications in diverse fields, such as materials science, where they can contribute to the development of advanced materials with enhanced performance characteristics.

The incorporation of the cinnoline moiety and the carboxylate group in Methyl cinnoline-6-carboxylate allows for the exploration of new synthetic pathways and the generation of diverse molecular scaffolds. This versatility empowers researchers to push the boundaries of chemical innovation, unlocking new possibilities in areas ranging from functional materials to energy-efficient technologies.

Handling and Safety Considerations

Methyl cinnoline-6-carboxylate is classified as a hazardous substance, with a hazard class of 14.1.5. It is associated with several hazard statements, including H302 (Harmful if swallowed), H315 (Causes skin irritation), H319 (Causes serious eye irritation), and H335 (May cause respiratory irritation). Appropriate safety measures must be taken when handling this compound, such as wearing protective gloves, clothing, eye protection, and ensuring adequate ventilation.

It is crucial to follow the prescribed P-statements, which outline the necessary precautions, first aid measures, and disposal guidelines. Researchers and laboratory personnel must familiarize themselves with the safety data sheet (SDS) and adhere to the recommended handling and storage protocols to ensure the safe and responsible use of Methyl cinnoline-6-carboxylate.

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Specifications
  • Class: 14.1.5
  • H statements: H302:Harmful if swallowed.H315:Causes skin irritation.H319:Causes serious eye irritation.H335:May cause respiratory irritation.
  • Inchi key: InChIKey=JMLKGGQGRGKUFU-UHFFFAOYSA-N
  • Molecular weight: 188.18600463867188
  • Notes: This product is intended for laboratory use only, and it is not meant for human consumption.Signal word: Warning
  • P statements: P261:Avoid breathing dust, fumes, gas, mist, vapours, spray. [As modified by IV ATP].P264:Wash thoroughly after handling.P270:Do not eat, drink or smoke when using this product.P271:Use only outdoors or in a well-ventilated area.P280:Wear protective glove
  • Purity: 95.0%
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