2-Bromothiophene: Properties, Applications, and Sourcing for Chemical R&D
For researchers and scientists engaged in chemical R&D, the availability of versatile and high-quality building blocks is paramount to exploring new frontiers in synthesis and material science. 2-Bromothiophene (CAS: 1003-09-4) stands out as a particularly valuable compound due to its unique structure and reactivity. This article provides an essential overview for R&D professionals, detailing its chemical properties, diverse applications, and guidance on how to effectively source this key intermediate.
The Chemical Identity of 2-Bromothiophene
2-Bromothiophene is an organobromine compound derived from thiophene, a sulfur-containing aromatic heterocycle. Its molecular formula is C4H3BrS, with a molecular weight of 163.04. It typically appears as a clear, colorless to pale yellow liquid, possessing a distinct odor. Key physical characteristics include a boiling point of approximately 149-151 °C and a density of around 1.684 g/mL at 25 °C. Its miscibility profile indicates it is immiscible with water but readily dissolves in common organic solvents like diethyl ether and acetone. The compound is also light-sensitive, necessitating storage in appropriate, sealed containers away from direct light to maintain its integrity.
The compound's CAS number, 1003-09-4, serves as a unique identifier, simplifying searches for suppliers and technical information. For R&D purposes, the purity of 2-Bromothiophene is a critical parameter, with high-purity grades (≥99%) often preferred to ensure the predictability and success of complex synthetic endeavors.
Versatile Applications in Research and Synthesis
While 2-Bromothiophene is widely recognized for its role as an intermediate in the synthesis of pharmaceuticals, such as the antiplatelet drug Clopidogrel, its utility extends broadly across various R&D disciplines:
- Organic Synthesis: Its structure makes it an excellent substrate for a range of reactions, including Grignard reactions, palladium-catalyzed cross-coupling reactions (e.g., Suzuki, Stille, Heck), and lithiation followed by electrophilic quench. These reactions allow for the introduction of diverse functional groups onto the thiophene ring.
- Material Science: Thiophene derivatives are integral to the development of advanced materials, particularly in organic electronics. 2-Bromothiophene can be used as a monomer or building block for conjugated polymers and oligomers with conductive or semiconductive properties, relevant for organic thin-film transistors (OTFTs), organic photovoltaics (OPVs), and organic light-emitting diodes (OLEDs).
- Medicinal Chemistry: Beyond established drugs, chemists use 2-Bromothiophene to synthesize novel chemical entities for drug discovery programs, exploring its potential in various therapeutic areas.
- Catalysis Research: As a thiophene-based compound, it can be involved in research related to organometallic catalysts or ligands.
For R&D scientists, the ability to easily buy 2-bromothiophene in quantities suitable for laboratory scale experiments is essential. Accessing reliable manufacturers and suppliers who cater to the research community is key.
Strategic Sourcing for R&D
When sourcing 2-Bromothiophene for research and development, scientists should:
- Prioritize Purity: Opt for grades with assay ≥99% to avoid interference in sensitive reactions.
- Seek Reputable Suppliers: Look for manufacturers or distributors with a strong online presence and clear product information, including CAS numbers and specifications.
- Request Samples: If available, ordering small sample quantities can be beneficial for initial testing and validation.
- Compare Pricing and Availability: Even for R&D, understanding market prices and lead times is important for project planning.
In conclusion, 2-Bromothiophene is a chemical workhorse for the modern R&D laboratory. Its versatile reactivity and application in cutting-edge fields like material science and medicinal chemistry make it an invaluable intermediate. By understanding its properties and adopting a strategic approach to sourcing, R&D professionals can ensure they have a reliable supply of this essential compound to drive their innovative projects forward.
Perspectives & Insights
Molecule Vision 7
“The compound is also light-sensitive, necessitating storage in appropriate, sealed containers away from direct light to maintain its integrity.”
Alpha Origin 24
“The compound's CAS number, 1003-09-4, serves as a unique identifier, simplifying searches for suppliers and technical information.”
Future Analyst X
“For R&D purposes, the purity of 2-Bromothiophene is a critical parameter, with high-purity grades (≥99%) often preferred to ensure the predictability and success of complex synthetic endeavors.”