Unlocking Synthetic Potential: The Versatility of 4-Bromo-1-butene in Organic Chemistry
Organic chemistry is the art and science of building molecules, and the availability of versatile building blocks is essential for creative synthesis. 4-Bromo-1-butene (CAS 5162-44-7) is one such compound, offering chemists a powerful tool due to its unique combination of a reactive bromine atom and a terminal alkene. As a chemical manufacturer with a strong focus on fine chemicals and pharmaceutical intermediates, we are proud to offer high-purity 4-Bromo-1-butene to the global scientific community.
The chemical structure of 4-Bromo-1-butene makes it an ideal substrate for a multitude of organic transformations. Its reactivity stems from the relatively labile C-Br bond, making it an excellent electrophile in nucleophilic substitution reactions. This allows for the introduction of the 3-butenyl moiety into various organic frameworks. For example, reaction with Grignard reagents or organolithium compounds can lead to the formation of new carbon-carbon bonds. Similarly, it can participate in palladium-catalyzed cross-coupling reactions, such as Suzuki, Heck, or Sonogashira couplings, further expanding its synthetic utility.
The presence of the alkene functionality opens up another avenue for chemical modification. This double bond can undergo a variety of addition reactions, including hydrogenation, epoxidation, dihydroxylation, or Diels-Alder reactions. In conjunction with the bromine atom, this allows for sequential functionalization strategies. For instance, one might first utilize the bromine for an alkylation and then modify the alkene via oxidation or reduction, creating complex molecules with precise control over stereochemistry and functionality.
In the realm of pharmaceutical synthesis, 4-Bromo-1-butene is a valued intermediate. Its ability to introduce a specific carbon chain length with latent reactivity is crucial for building the scaffolds of many drug candidates. Researchers investigating new therapeutic agents often rely on such building blocks to efficiently construct libraries of compounds for screening. When you decide to buy 4-Bromo-1-butene from a reputable supplier like us, you ensure that your synthesis efforts are supported by a reliable source of high-quality material.
For scientists and procurement managers looking to leverage the synthetic potential of 4-Bromo-1-butene, sourcing from a trusted manufacturer in China is often a prudent choice. Our commitment to quality control and competitive pricing ensures that you receive a superior product without overextending your budget. We understand that consistent supply is critical for ongoing research and development. Therefore, we maintain robust production capabilities and efficient logistics to serve your needs.
We invite you to explore the possibilities that 4-Bromo-1-butene offers for your next synthetic challenge. Contact us to obtain a detailed quote and discuss how our high-purity CAS 5162-44-7 can empower your chemical innovation. Discover the difference that a reliable, quality-focused supplier can make to your research and production workflows.
Perspectives & Insights
Agile Reader One
“For example, reaction with Grignard reagents or organolithium compounds can lead to the formation of new carbon-carbon bonds.”
Logic Vision Labs
“Similarly, it can participate in palladium-catalyzed cross-coupling reactions, such as Suzuki, Heck, or Sonogashira couplings, further expanding its synthetic utility.”
Molecule Origin 88
“The presence of the alkene functionality opens up another avenue for chemical modification.”