3-[3-(Trifluoromethyl)phenyl]-1,2-thiazole-4-sulfonyl chloride - 250mg

REF #: 3D-JBD33734
Short description

3-[3-(Trifluoromethyl)phenyl]-1,2-thiazole-4-sulfonyl chloride

Discover the versatility of 3-[3-(Trifluoromethyl)phenyl]-1,2-thiazole-4-sulfonyl chloride, a high-purity (Min. 95%) chemical compound with a molecular weight of 327.7 g/mol. This unique thiazole derivative, bearing the CAS number 1909337-34-3, offers a powerful tool for your advanced research and synthesis needs. Its trifluoromethyl group and sulfonyl chloride functionality provide a rich canvas for diverse chemical transformations, unlocking a world of possibilities in the fields of pharmaceuticals, agrochemicals, and beyond. Handle with care, as this compound may cause skin and eye irritation, and always store in a cool, well-ventilated area. Embrace the precision and performance of this exceptional chemical in your next groundbreaking project.

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

3-[3-(Trifluoromethyl)phenyl]-1,2-thiazole-4-sulfonyl chloride

Unlock the versatile potential of 3-[3-(Trifluoromethyl)phenyl]-1,2-thiazole-4-sulfonyl chloride, a highly specialized chemical compound that holds the key to unlocking new frontiers in scientific research and development. This meticulously crafted molecule, identified by its CAS number 1909337-34-3, boasts a unique combination of structural features that make it a valuable asset in a wide range of applications.

At the heart of this compound lies a 1,2-thiazole core, adorned with a 3-(trifluoromethyl)phenyl substituent and a sulfonyl chloride functional group. This intricate molecular architecture endows 3-[3-(Trifluoromethyl)phenyl]-1,2-thiazole-4-sulfonyl chloride with exceptional chemical reactivity and versatility, making it a sought-after building block in the realms of pharmaceutical research, agrochemical development, and beyond.

Pharmaceutical Prowess

In the dynamic world of pharmaceutical research, this compound shines as a crucial starting material and versatile reagent. Its unique structural features allow for the synthesis of a wide range of innovative drug candidates, targeting a diverse array of therapeutic areas. From neurological disorders to metabolic conditions, the potential applications of 3-[3-(Trifluoromethyl)phenyl]-1,2-thiazole-4-sulfonyl chloride in the pharmaceutical industry are vast and promising.

The presence of the trifluoromethyl group, a hallmark of this compound, enhances its lipophilicity and metabolic stability, crucial factors in the development of effective and well-tolerated pharmaceuticals. Additionally, the sulfonyl chloride moiety serves as a reactive handle, enabling the incorporation of diverse functional groups and the creation of tailored molecular structures with enhanced pharmacological profiles.

Agrochemical Innovations

Beyond the realm of pharmaceuticals, 3-[3-(Trifluoromethyl)phenyl]-1,2-thiazole-4-sulfonyl chloride also finds its place in the dynamic field of agrochemical development. Its unique chemical properties contribute to the synthesis of advanced crop protection agents, including potent and selective pesticides.

The trifluoromethyl group, a hallmark of this compound, enhances its lipophilicity and metabolic stability, crucial factors in the development of effective and well-tolerated agrochemicals. Additionally, the sulfonyl chloride moiety serves as a reactive handle, enabling the incorporation of diverse functional groups and the creation of tailored molecular structures with enhanced efficacy and specificity, ultimately leading to healthier crops and higher yields.

Versatile Chemical Synthesis

Beyond its pharmaceutical and agrochemical applications, 3-[3-(Trifluoromethyl)phenyl]-1,2-thiazole-4-sulfonyl chloride is a valuable tool in the realm of chemical synthesis. Its distinct structural features and reactivity make it a versatile building block for the creation of novel compounds with tailored properties, opening up new avenues for material science, organic synthesis, and beyond.

The combination of the trifluoromethyl group, the 1,2-thiazole core, and the sulfonyl chloride functionality endows this compound with a unique chemical profile, allowing it to participate in a wide range of synthetic transformations. Researchers and chemists can leverage the versatility of 3-[3-(Trifluoromethyl)phenyl]-1,2-thiazole-4-sulfonyl chloride to unlock new possibilities in their respective fields, driving scientific progress and innovation.

Technical Specifications

  • Name: 3-[3-(Trifluoromethyl)phenyl]-1,2-thiazole-4-sulfonyl chloride
  • CAS Number: 1909337-34
Specifications
  • Formula: C10H5ClF3NO2S2
  • Mdl: MFCD29762870
  • Molecular weight: 327.7 g/mol
  • Purity: Min. 95%
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