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Description
Ethyl (R)-4-Chloro-3-hydroxybutanoate is a chiral building block widely used in asymmetric synthesis to construct molecules with specific biological activities. This compound plays a crucial role in organic chemistry laboratories by enabling the creation of complex molecular structures with defined stereochemistry. Its unique chemical structure, featuring both a hydroxyl group and a chloro substituent, makes it highly reactive and suitable for various synthetic transformations. As a key component in the development of pharmaceuticals and bioactive compounds, this material is essential for researchers aiming to achieve precise control over molecular configuration.
The compound’s chiral nature and functional groups contribute to its versatility in synthetic applications. Its ability to participate in multiple chemical reactions allows it to be a valuable tool in the synthesis of enantiomerically pure compounds. The presence of the hydroxyl group enhances its reactivity, making it suitable for a range of chemical modifications. Additionally, its structural characteristics enable it to serve as a versatile intermediate in the preparation of various pharmaceutical and agrochemical compounds. These properties make it a preferred choice for chemists working in both academic and industrial settings.
In Indonesian laboratories, Ethyl (R)-4-Chloro-3-hydroxybutanoate is commonly used in organic chemistry research, particularly in the field of asymmetric synthesis. It is frequently employed in the development of bioactive compounds and pharmaceuticals, where precise stereochemical control is essential. Many research institutions and universities in Indonesia utilize this compound for synthetic studies, contributing to advancements in medicinal chemistry and chemical innovation.
Laboratory Applications
Asymmetric synthesis is a key application where this compound enables the creation of enantiomerically pure molecules, crucial for pharmaceutical development.
Organic chemistry research benefits from its reactivity and chiral structure, allowing for the synthesis of complex molecular frameworks.
Pharmaceutical compound development relies on its ability to provide stereochemical control, essential for designing drugs with specific biological activities.
Bioactive molecule synthesis utilizes its functional groups to facilitate various chemical transformations in synthetic pathways.
Academic research in chemical sciences employs it to explore new synthetic methods and understand stereochemical behavior in molecular structures.
Specifications
Brand: TCI
CAS number: 90866-33-4
Category: Chemistry > Asymmetric Synthesis > Chiral Building Blocks
Pack sizes: Available in various quantities as per supplier specifications
Physical form: Liquid or solid, depending on the specific formulation
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 location, away from direct light and moisture to maintain its stability and purity. It is recommended to use airtight containers made of glass or high-density polyethylene to prevent contamination and degradation. Due to its reactive nature, it should be handled with care, using appropriate personal protective equipment such as gloves and safety goggles. In laboratory settings, it is important to ensure proper ventilation to minimize exposure to vapors. Avoid contact with incompatible substances, and always follow standard safety protocols when working with chiral building blocks. Proper storage and handling are essential to preserve the compound’s integrity and ensure safe usage in research applications.
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