Understanding the Chemical Properties of 1-Bromo-4-iodobutane for Synthesis
In the intricate world of organic synthesis, understanding the fundamental properties and reactivity of intermediate compounds is key to successful outcomes. 1-Bromo-4-iodobutane (CAS: 89044-65-5) stands out as a highly valuable bifunctional molecule, prized for its dual halogen substitution and predictable chemical behavior. This article explores the chemical characteristics of this compound and highlights why it is a preferred choice for researchers and manufacturers in various chemical sectors.
Chemical Profile of 1-Bromo-4-iodobutane
1-Bromo-4-iodobutane is a colorless liquid with the molecular formula C4H8BrI and a molecular weight of approximately 262.91 g/mol. Its defining feature is the presence of both a bromine atom and an iodine atom at opposite ends of a four-carbon aliphatic chain. This structural arrangement dictates its reactivity and utility in synthesis:
- Differential Reactivity of Halogens: The carbon-iodine bond is generally weaker and more reactive than the carbon-bromine bond. This difference allows for selective reactions, where the iodine can be preferentially substituted or reacted while leaving the bromine intact for subsequent transformations.
- Nucleophilic Substitution Reactions: Both halogens can undergo nucleophilic substitution, allowing for the introduction of various functional groups such as alcohols, amines, or ethers.
- Organometallic Reagent Formation: It can be used to form Grignard reagents or organolithium compounds, which are powerful tools in carbon-carbon bond formation.
- Cross-Coupling Reactions: While its aliphatic nature limits direct participation in typical aryl cross-coupling, derivatives can be synthesized for such purposes, or it can be used in alkyl cross-coupling reactions.
Applications Driven by Chemical Properties
The unique reactivity of 1-Bromo-4-iodobutane makes it an indispensable tool for chemists aiming to synthesize complex organic molecules. Its utility is particularly noted in:
- Pharmaceutical Intermediates: Facilitating the synthesis of drug molecules with precise structural requirements.
- Agrochemical Synthesis: Enabling the creation of effective pesticides and herbicides.
- Research and Development: A fundamental building block for exploring new synthetic methodologies and discovering novel compounds.
For those looking to purchase 1-bromo-4-iodobutane, partnering with a quality-focused organic synthesis raw materials manufacturer is essential. Ensuring a consistent supply of high-purity material from a reliable 1-bromo-4-iodobutane supplier China-based can significantly enhance your R&D and production capabilities. Understanding its chemical properties empowers chemists to leverage this compound effectively in their synthetic strategies.
Perspectives & Insights
Future Origin 2025
“This difference allows for selective reactions, where the iodine can be preferentially substituted or reacted while leaving the bromine intact for subsequent transformations.”
Core Analyst 01
“Nucleophilic Substitution Reactions: Both halogens can undergo nucleophilic substitution, allowing for the introduction of various functional groups such as alcohols, amines, or ethers.”
Silicon Seeker One
“Organometallic Reagent Formation: It can be used to form Grignard reagents or organolithium compounds, which are powerful tools in carbon-carbon bond formation.”