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The Strategic Advantage of 3-Bromo-2-iodothiophene in Modern Synthesis

In the intricate world of chemical synthesis, the ability to precisely control reactions is paramount. For researchers and procurement managers in the B2B chemical sector, identifying versatile building blocks that offer high regioselectivity and reliability is key to innovation and cost-efficiency. Among these crucial compounds, 3-Bromo-2-iodothiophene stands out as a powerful tool, enabling sophisticated molecular constructions. As a dedicated manufacturer and supplier, we understand the strategic value this intermediate brings to diverse industries.

3-Bromo-2-iodothiophene, identified by CAS number 60404-24-2, possesses a unique structural characteristic: two different halogen atoms attached to the thiophene ring. This difference in halogenation is not merely an academic detail; it forms the bedrock of its synthetic utility. The carbon-iodine (C-I) bond is generally more reactive than the carbon-bromine (C-Br) bond in many common organic reactions, particularly in palladium-catalyzed cross-coupling reactions such as Suzuki-Miyaura, Stille, and Sonogashira couplings. This differential reactivity allows chemists to perform sequential functionalization, selectively modifying one position on the thiophene ring while leaving the other intact for subsequent transformations. This 'orthogonal reactivity' is invaluable for constructing complex, unsymmetrical molecules with high precision.

Procurement managers seeking this essential chemical will find that reliable manufacturers in China offer not only competitive pricing but also consistent quality. The ability to buy 3-Bromo-2-iodothiophene in bulk from a trusted source ensures a stable supply chain, a critical factor for production timelines. Furthermore, custom synthesis services can be leveraged to obtain specific derivatives or higher purity grades tailored to unique project requirements.

The applications of 3-Bromo-2-iodothiophene span several high-value sectors. In materials science, it is a cornerstone for synthesizing conjugated polymers and small molecules essential for organic electronics. These materials are the backbone of innovations in organic light-emitting diodes (OLEDs), organic field-effect transistors (OFETs), and organic solar cells (OSCs). The ability to precisely engineer the electronic and optical properties of these materials often hinges on the controlled incorporation of thiophene units derived from such versatile intermediates.

In the pharmaceutical industry, the thiophene ring is a common and valuable scaffold. Its structural similarity to phenyl rings, coupled with its unique electronic properties, allows it to interact effectively with biological targets. 3-Bromo-2-iodothiophene serves as a key starting material for building more complex heterocyclic systems that form the basis of novel drug candidates. The strategic placement of functional groups, facilitated by the regioselective nature of reactions involving this compound, is crucial in the drug discovery process, from lead optimization to the synthesis of active pharmaceutical ingredients (APIs).

For research scientists, understanding the reactivity profile of 3-Bromo-2-iodothiophene is essential. Its participation in organometallic reactions, such as lithium-halogen exchange, opens up pathways for introducing a wide array of functional groups. The preferential exchange at the iodine-bearing position is a well-established phenomenon, enabling the formation of stable organolithium or Grignard reagents that can then react with various electrophiles. This controlled reactivity minimizes side reactions and maximizes the yield of the desired product, a factor that directly impacts research efficiency and budget.

In conclusion, 3-Bromo-2-iodothiophene is more than just a chemical compound; it is a strategic enabler for innovation. Its unique halogenation pattern provides unparalleled control over synthetic pathways, making it indispensable for creating advanced materials and novel pharmaceuticals. As a leading manufacturer and supplier, we are committed to providing researchers and businesses with high-quality 3-Bromo-2-iodothiophene, backed by expertise and a dedication to customer success. Whether you are looking to buy in bulk, require custom synthesis, or simply need a reliable supplier, we are your partner in chemical excellence.

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NINGBO INNO PHARMCHEM CO.,LTD. was established in 2007. It is committed to the R&D, production and sales of raw materials, pharmaceutical intermediates and fine chemicals. We striving to create a high-efficiency and high-quality integrated chemical service platform to better serve domestic and foreign customers.

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2. Own R&D laboratory, pilot platform and large-scale production workshop, which can meet the audit requirements of global customers;

3. We can satisfy customers' perfect transition from small scale lab requirements (gram level) to commercialization requirements (hundred tons level).

FAQ

  • A: We don't have Minimum Order Quantity, exact quantity should be provided before quotation for us to calculate the exact cost.

  • A: We don't provide free samples due to lots of request and expensive international courier's cost, we can deduct the sample charge after commercial order placed.

  • A: Our payment terms: Small or sample order: T/T IN ADVANCE. Commercial order: First order should be by T/T IN ADVANCE or L/C at sight, and following orders T/T 30~90days is acceptable subject to approval of credit application.

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