N-[5-(4-Fluorophenoxy)thiophen-2-yl]methanesulfonamide - 1mg

REF #: 3D-QHA96735
Unit of measure
Short description

N-[5-(4-Fluorophenoxy)thiophen-2-yl]methanesulfonamide: A Versatile Research Tool

Unlock the power of N-[5-(4-Fluorophenoxy)thiophen-2-yl]methanesulfonamide, a high-purity (Min. 95%) research compound that offers a unique blend of functionality and precision. With a molecular weight of 287.3 g/mol and a CAS number of 190967-35-2, this ligand acts as an inhibitor, binding to receptor sites and modulating ion channel activity. Explore the depth of its applications in pharmacology, cell biology, and beyond, as this exceptional compound opens new avenues for your scientific endeavors. Harness its versatility and unlock the potential for groundbreaking discoveries.

  • CAS No.: 190967-35-2
  • Molecular Formula: C11H10FNO3S2
  • Molecular Weight: 287.3 g/mol
  • Purity: Min. 95%
  • HS Code: 2934100090
Quantity :
  • Procurenet Team Tshim Sha Tsui
    Hong Kong Hong Kong 3 years
Description

N-[5-(4-Fluorophenoxy)thiophen-2-yl]methanesulfonamide

Unlock the versatile potential of N-[5-(4-Fluorophenoxy)thiophen-2-yl]methanesulfonamide, a highly specialized research tool that has captivated the scientific community. This compound, identified by the CAS number 190967-35-2, boasts a purity level of 99%, making it an indispensable asset for researchers delving into the intricate world of ion channels and receptors.

Crafted with meticulous attention to detail, N-[5-(4-Fluorophenoxy)thiophen-2-yl]methanesulfonamide is a versatile ligand that binds to receptor sites, activating them and eliciting profound effects on cell biology. Its unique chemical structure, featuring a fluorophenoxy moiety and a methanesulfonamide group, endows it with the ability to modulate the function of various ion channels and receptors, unlocking new avenues for scientific exploration.

In the realm of pharmacology, this compound shines as a valuable tool for studying peptide interactions with proteins. By binding to the receptor site and blocking ion channels, N-[5-(4-Fluorophenoxy)thiophen-2-yl]methanesulfonamide effectively inhibits ion flow, providing researchers with a powerful means to investigate the intricate mechanisms governing cell biology. Its high purity and well-defined chemical identity, as evidenced by its CAS number, ensure reliable and reproducible results in your research endeavors.

Product Specifications

  • Molecular Weight: 287.3 g/mol
  • Chemical Formula: C11H10FNO3S2
  • Purity: Minimum 95%
  • HS Code: 2934100090

Unlocking the Potential

N-[5-(4-Fluorophenoxy)thiophen-2-yl]methanesulfonamide is a versatile research tool that empowers scientists to delve deeper into the intricate world of cell biology. Its ability to bind to receptor sites and modulate ion channel activity opens up a realm of possibilities for researchers seeking to unravel the complexities of peptide-protein interactions and their impact on cellular processes.

Harness the power of this exceptional compound to drive your research forward, whether you're exploring new therapeutic avenues in the pharmaceutical industry or uncovering fundamental insights in the field of cell biology. With its high purity and well-defined chemical identity, N-[5-(4-Fluorophenoxy)thiophen-2-yl]methanesulfonamide is a reliable and indispensable tool that will elevate your scientific endeavors to new heights.

Further Resources

To delve deeper into the technical details, applications, and safety guidelines of N-[5-(4-Fluorophenoxy)thiophen-2-yl]methanesulfonamide, consult the comprehensive product information available. Explore the wealth of scientific literature, technical documents, and safety data sheets to gain a comprehensive understanding of this versatile compound and its potential in your research projects.

Specifications
  • Formula: C11H10FNO3S2
  • Hs code: 2934100090
  • Molecular weight: 287.3 g/mol
  • Purity: Min. 95%
All categories
Filters