(R)-(-)-2-Chloro-1-phenylethanol is a chiral compound widely used in asymmetric synthesis to construct molecules with specific biological activity. This compound plays a crucial role in organic chemistry laboratories, where it serves as a key building block for creating complex molecular structures. Its optical activity makes it particularly valuable in research focused on drug development and the synthesis of bioactive compounds. Due to its unique stereochemistry, it is essential for producing enantiomerically pure substances, which are critical in pharmaceutical and biochemical applications.
The compound's molecular structure, featuring a phenyl group and a chloro substituent on an ethyl chain, contributes to its high reactivity and versatility in chemical reactions. These properties make it a preferred choice for researchers aiming to explore various synthetic pathways. Its ability to participate in multiple reaction mechanisms enhances its utility in both academic and industrial settings. Additionally, its stability under controlled conditions ensures reliable performance in laboratory experiments.
In Indonesian laboratories, (R)-(-)-2-Chloro-1-phenylethanol is commonly used in organic chemistry research, especially in pharmacology, biochemistry, and the synthesis of complex compounds. Researchers in educational institutions and research centers rely on this compound for experiments requiring precise stereochemical control. Its availability through suppliers like AMI Scientific supports ongoing scientific inquiry and innovation in the field.
- Asymmetric synthesis is a key application where this compound enables the creation of enantiomerically pure molecules, essential for pharmaceutical development.
- Organic chemistry research benefits from its reactivity and stereochemistry, allowing the synthesis of complex bioactive compounds.
- Pharmaceutical development relies on its ability to produce chiral intermediates, which are crucial for drug molecule design.
- Biochemical studies utilize its optical activity to investigate enzyme interactions and molecular recognition processes.
- Industrial chemical synthesis incorporates it for the production of specialty chemicals with specific stereochemical properties.
| Brand | TCI |
|---|---|
| CAS number | 56751-12-3 |
| Molecular formula | — |
| Purity | — |
| Category | Chemistry > Asymmetric Synthesis > Chiral Building Blocks |
| Pack sizes | Available in various quantities as per supplier specifications |
| Physical form | Liquid |
| Storage | Store in a cool, dark place away from moisture and light |
This compound should be stored in a cool, dark environment to maintain its stability and prevent degradation. It is recommended to use airtight containers to minimize exposure to moisture and air, which can affect its chemical integrity. Due to its potential reactivity, it should be handled in a well-ventilated area, preferably under a fume hood, to ensure safety. Proper personal protective equipment, including gloves and safety goggles, should be worn during handling. The compound should be kept away from incompatible materials such as strong oxidizers. Regular monitoring of storage conditions is essential to preserve its quality and effectiveness in laboratory applications.
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