High Purity 2-Bromo-1,3,5-triisopropylbenzene CAS: 21524-34-5 for Advanced Chemical Synthesis
Discover a crucial organic intermediate for your next breakthrough in Suzuki reactions and complex molecule synthesis.
Get a Quote & SampleProduct Core Value
2-Bromo-1,3,5-triisopropylbenzene
2-Bromo-1,3,5-triisopropylbenzene is a critical aryl bromide utilized extensively as a building block in organic synthesis. Its well-defined chemical structure and high purity make it an ideal reagent for Suzuki reactions and other cross-coupling methodologies, enabling the efficient construction of complex organic molecules.
- Leveraging 2-bromo-1,3,5-triisopropylbenzene synthesis capabilities, researchers can access this vital compound for novel research.
- Understanding the CAS 21524-34-5 chemical properties is key to optimizing its use in various reaction pathways.
- As an organic synthesis building block, it offers versatility in creating diverse molecular architectures.
- Its application in Suzuki reactions ensures efficient carbon-carbon bond formation, a cornerstone of modern organic chemistry.
Advantages Provided by the Product
Enhanced Reaction Efficiency
The specific structure of this aryl bromide contributes to improved yields and selectivity in reactions, a crucial aspect for complex organic synthesis.
Synthetic Versatility
As a fine chemical, it serves as a versatile intermediate, facilitating the synthesis of a wide array of advanced organic compounds.
Reliable Supply Chain
Sourcing from reputable suppliers ensures consistent quality and availability of this important chemical intermediate for ongoing projects.
Key Applications
Organic Synthesis
As a key intermediate, it is essential for building complex organic molecules, supporting advancements in medicinal chemistry and material science.
Suzuki Reaction
This compound is a vital component in Suzuki-Miyaura coupling reactions, a widely used method for creating carbon-carbon bonds in the synthesis of pharmaceuticals and advanced materials.
Ring Closure Reactions
Its participation in highly selective ring closures, such as those involving homoallylic alcohols, leads to the formation of substituted tetrahydrofurans.
Material Science Research
The unique structure of this aryl bromide makes it a candidate for developing novel materials with specific electronic or optical properties.