For organic chemists, the selection of appropriate building blocks can dramatically influence the efficiency, yield, and overall success of a synthesis project. 2-Iodothiophene (CAS: 3437-95-4) is a highly versatile organosulfur compound that plays a critical role in numerous synthetic strategies, particularly those involving the formation of carbon-carbon and carbon-heteroatom bonds.

Understanding the Reactivity of 2-Iodothiophene

The presence of the iodine atom on the thiophene ring makes 2-Iodothiophene an excellent electrophile in cross-coupling reactions. This characteristic is fundamental for its widespread use in synthesizing complex organic molecules. The C-I bond is readily activated by transition metal catalysts, such as palladium or nickel, enabling the formation of new bonds with organometallic reagents, amines, and other nucleophiles.

Key synthetic transformations involving 2-Iodothiophene include:

  • Suzuki-Miyaura Coupling: Reacting with organoboron compounds to form C-C bonds.
  • Stille Coupling: Coupling with organotin compounds for C-C bond formation.
  • Sonogashira Coupling: Reacting with terminal alkynes to introduce alkyne functionalities.
  • Heck Reaction: Coupling with alkenes.
  • Buchwald-Hartwig Amination: Forming C-N bonds by reacting with amines.

These reactions are indispensable for constructing conjugated systems, creating intricate scaffolds for pharmaceuticals, agrochemicals, and advanced materials. Researchers often seek to 'buy 2-iodothiophene' for its predictable reactivity and broad applicability in these transformations.

Efficient Synthesis Routes for 2-Iodothiophene

While 2-Iodothiophene is commercially available, understanding its synthesis can be beneficial for process chemists. Established procedures, such as those found in Organic Syntheses, detail methods involving the direct iodination of thiophene using iodine in the presence of mercuric oxide or nitric acid. Another efficient route involves a halogen exchange from 2-chlorothiophene using sodium iodide in a polar aprotic solvent. The choice of synthesis method often depends on desired purity levels and scalability. When purchasing, always confirm the CAS number (3437-95-4) and inquire about the purity specifications, which are typically 97% or higher.

Sourcing 2-Iodothiophene: A Manufacturer's Perspective

As a dedicated manufacturer and supplier, we pride ourselves on providing high-quality 2-Iodothiophene to the global market. Our commitment to stringent quality control ensures that chemists receive a reliable intermediate for their demanding synthetic projects. When you need to buy this compound, consider partnering with a supplier like us that offers consistent purity, competitive pricing, and excellent customer support. Many buyers search for '2-iodothiophene price' or 'order 2-iodothiophene online' to find cost-effective solutions.

By choosing a reliable source for 2-Iodothiophene, you can streamline your synthetic workflows and achieve superior results. We are ready to meet your requirements. Contact us today for a quote or to discuss your organic synthesis needs.