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Description
(R)-1-(4-Fluorophenyl)ethan-1-ol is a chiral building block widely used in asymmetric synthesis, playing a crucial role in the development of complex organic molecules. This compound is essential for creating chiral compounds with specific biological activities, making it a key component in pharmaceutical research. Its unique molecular structure, featuring a fluorine group on the phenyl ring, allows for precise control over stereochemistry during chemical reactions. This makes it particularly valuable in the synthesis of drugs and other bioactive compounds.
The compound's chiral nature and fluorinated phenyl group contribute to its effectiveness in asymmetric synthesis. Its ability to participate in various chemical transformations while maintaining stereochemical integrity makes it a preferred choice for chemists working on enantioselective processes. The presence of the fluorine atom also enhances its reactivity and selectivity in different reaction conditions. These properties make it ideal for applications requiring high specificity and controlled molecular structure.
In Indonesian laboratories, this compound is commonly used in organic chemistry research, especially in pharmacology and the development of new chemical compounds. It is a staple in academic and industrial research settings, where its role in creating chiral molecules is critical. Its application is widespread in drug discovery and the synthesis of bioactive substances, supporting advancements in both academic and applied research.
Laboratory Applications
Asymmetric Synthesis: This compound is ideal for creating chiral molecules with specific stereochemistry, essential for drug development and bioactive compound synthesis.
Pharmaceutical Research: Its chiral structure makes it valuable for developing new drugs with targeted biological activities and improved therapeutic effects.
Organic Chemistry Studies: It is frequently used in academic research to explore reaction mechanisms and stereochemical outcomes in complex molecular transformations.
Bioactive Compound Development: The fluorinated phenyl group enhances reactivity, making it useful for synthesizing compounds with specific biological functions.
Chiral Separation Processes: Its chiral nature aids in the separation of enantiomers, a critical step in producing pure, active pharmaceutical ingredients.
Specifications
Brand: TCI
CAS number: 101219-68-5
Category: Chemistry > Asymmetric Synthesis > Chiral Building Blocks
Pack sizes: Available in various quantities as per supplier specifications
Physical form: Liquid or crystalline, depending on purity and storage conditions
Storage note: Store in a cool, dry place away from light and moisture
Handling and Storage
This compound should be stored in a cool, dry environment, away from direct light and moisture to maintain its chemical integrity. It is recommended to use airtight, sealed containers made of materials compatible with organic solvents to prevent contamination and degradation. Due to its chiral nature, it is important to handle it with care to avoid any unintended stereochemical changes during synthesis. Proper labeling and storage conditions are essential to ensure its stability and usability in laboratory settings. Always follow standard safety protocols when handling chemical substances to minimize risks and ensure a safe working environment.
