4-[(Difluoromethyl)thio]benzene-1,2-diamine -

REF #: 54-PC50146
Short description

4-[(Difluoromethyl)thio]benzene-1,2-diamine: A Versatile Fluorinated Compound

Discover the exceptional 4-[(Difluoromethyl)thio]benzene-1,2-diamine, a versatile fluorinated compound with a CAS number of 1221278-43-8. This unique chemical boasts a molecular weight of 190.21g/mol, offering a powerful tool for your advanced research and development needs. Crafted with precision, it presents a clear path to unlocking new possibilities in the realm of fluorinated compounds. Explore its diverse applications, from pharmaceuticals to agrochemicals, and witness the transformative impact it can have on your projects. Embrace the quality and reliability of this premium-grade product, and let it elevate your scientific endeavors to new heights.

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  • Procurenet Team Tshim Sha Tsui
    Hong Kong Hong Kong 3 years
Description

4-[(Difluoromethyl)thio]benzene-1,2-diamine

Introducing 4-[(Difluoromethyl)thio]benzene-1,2-diamine, a versatile and highly specialized Fluorinated Compound that holds immense potential for researchers and scientists across various disciplines. With its unique chemical structure and exceptional purity, this compound is poised to unlock new frontiers in pharmaceutical development, agrochemical innovation, and cutting-edge material science.

At the heart of this compound lies a captivating combination of a difluoromethylthio group and a 1,2-diamine moiety, granting it a distinct identity with the CAS number 1221278-43-8. Its molecular formula of C8H9F2N2S and a molecular weight of 190.21g/mol make it a valuable asset in the realm of organic synthesis and chemical research.

Pharmaceutical Prowess

In the dynamic world of pharmaceutical research, 4-[(Difluoromethyl)thio]benzene-1,2-diamine shines as a crucial building block for the development of innovative drug candidates. Its unique structural features allow for the synthesis of a wide range of therapeutic compounds, targeting a diverse array of health conditions. Researchers can leverage the compound's reactivity and selectivity to create novel pharmaceuticals with enhanced efficacy, improved pharmacokinetic profiles, and reduced side effects.

The difluoromethylthio group, in particular, has garnered significant attention for its ability to impart desirable properties to pharmaceutical molecules, such as increased metabolic stability, enhanced lipophilicity, and improved target binding affinity. By incorporating this versatile moiety into their synthetic strategies, pharmaceutical scientists can unlock new avenues for therapeutic breakthroughs.

Agrochemical Innovations

Beyond the realm of pharmaceuticals, 4-[(Difluoromethyl)thio]benzene-1,2-diamine also finds its place in the dynamic world of agrochemicals. Its distinct chemical structure and properties make it a valuable precursor in the development of advanced crop protection agents, including pesticides and herbicides.

The difluoromethylthio group, combined with the 1,2-diamine functionality, can contribute to the creation of highly selective and potent agrochemical compounds. These innovative formulations have the potential to enhance crop yields, protect against pests and diseases, and minimize environmental impact, all while adhering to the stringent regulatory requirements of the agrochemical industry.

Material Science Advancements

In the realm of material science, 4-[(Difluoromethyl)thio]benzene-1,2-diamine shines as a versatile building block for the synthesis of novel materials with tailored properties. Researchers can leverage the compound's unique chemical structure to engineer polymers, coatings, or other advanced materials with enhanced thermal stability, improved mechanical strength, or specialized optical characteristics.

The incorporation of the difluoromethylthio group and the 1,2-diamine moiety can impart desirable attributes to these materials, opening up new possibilities for applications in fields such as electronics, optoelectronics, and advanced composites. By harnessing the potential of this compound, material scientists can push the boundaries of innovation and create cutting-edge solutions to address the evolving needs of various industries.

Technical Specifications and Handling

4-[(Difluoromethyl)thio]benzene-1,2-diamine boasts a purity of 97%, ensuring reliable and consistent results in your research and development endeavors. Its chemical identity is further defined by the MDL number MFCD15147140 and the HS code 2930909899, providing a unique identifier and classification for international trade.

While the specific hazard information for this compound is yet to be confirmed (TBC), it is essential to handle it with the utmost care, adhering to standard laboratory safety protocols. This includes wearing appropriate personal protective equipment, working in a well-ventilated area, and following the recommended storage conditions to maintain the compound's stability and integrity over the long term.

Specifications
  • Hazard info: TBC
  • Hs code: 2930909899
  • Mdl: MFCD15147140
  • Molecular weight: 190.21g/mol
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