In the intricate world of fine chemicals, specific molecular structures act as linchpins for creating a vast array of specialized products. 4-Iodoacetophenone, scientifically known as 1-(4-iodophenyl)ethanone and bearing the CAS number 13329-40-3, stands out as one such versatile compound. Its unique chemical makeup, featuring an iodine atom in the para position of the acetophenone core, makes it an invaluable reagent for chemists engaged in advanced organic synthesis and the development of novel fine chemical products.

The Versatility of 4-Iodoacetophenone in Synthesis

The primary utility of 4-iodoacetophenone lies in its reactivity. The carbon-iodine bond is readily activated for various metal-catalyzed cross-coupling reactions, such as Suzuki, Heck, Sonogashira, and Buchwald-Hartwig couplings. These reactions are fundamental for constructing complex organic molecules, including those used in materials science, agrochemicals, and specialty polymers. Researchers and product formulators often seek to buy 4-iodoacetophenone to incorporate specific aromatic structures into their target molecules, thereby tuning properties like electronic behavior, solubility, or biological activity.

Sourcing High-Quality Intermediates: The Manufacturer's Role

For businesses in the fine chemical sector, sourcing reliable raw materials is as critical as the synthesis itself. When looking for 'CAS 13329-40-3 for sale,' it is essential to identify a manufacturer that can guarantee consistent quality and supply. A reputable 1-(4-iodophenyl)ethanone manufacturer in China can provide the necessary purity (typically ≥99%) and scale to meet production demands. Engaging with a supplier that understands the technical requirements of fine chemical synthesis ensures that the product will perform as expected, minimizing batch-to-batch variations and optimizing yields.

Key Applications in the Fine Chemical Industry

The applications of 4-iodoacetophenone are diverse and growing. It serves as a precursor in the synthesis of:

  • Advanced materials: Incorporating this moiety into polymers or organic electronic components can impart specific optical or conductive properties.
  • Agrochemicals: Certain crop protection agents and pesticides utilize complex aromatic structures derived from intermediates like 4-iodoacetophenone.
  • Specialty chemicals: It finds use in the creation of dyes, pigments, and additives where a functionalized aromatic ring is required.
  • Research chemicals: Its versatility makes it a staple for academic and industrial research laboratories exploring new synthetic pathways and molecular designs.

When considering the purchase of 4-iodoacetophenone, obtaining a detailed quotation from a trusted manufacturer is the first step. For those actively seeking to integrate this compound into their product lines, exploring reliable 1-(4-iodophenyl)ethanone suppliers will be a key factor in their supply chain strategy. The accessibility and quality offered by manufacturers can significantly impact the cost-effectiveness and success of fine chemical production.