(1,2)-1,2-Cyclohexanedimethanol is a chiral building block widely used in asymmetric synthesis within laboratory settings. This compound plays a crucial role in the development of complex molecular structures, particularly in the creation of bioactive compounds. Its unique structure, featuring two methanol groups attached to a cyclohexane ring, allows for precise control over stereochemistry during chemical reactions. This makes it an essential tool for researchers aiming to produce molecules with specific spatial configurations. Due to its stability and reactivity, it is frequently employed in synthetic pathways that require high selectivity and efficiency.
The compound’s chiral nature and structural symmetry make it a preferred choice for synthetic chemists. Its ability to serve as a chiral auxiliary enables the synthesis of enantiomerically pure compounds, which are vital in pharmaceutical and agrochemical research. The compound’s chemical stability ensures it remains effective across a range of reaction conditions, making it a reliable reagent in both academic and industrial laboratories. Additionally, its compatibility with various synthetic methodologies enhances its versatility in different experimental setups.
In Indonesian laboratories, (1,2)-1,2-Cyclohexanedimethanol is commonly used in organic chemistry research, especially in asymmetric synthesis and drug development. It is a key component in experiments that require precise control over molecular structure and stereochemistry. Many research institutions and universities in Indonesia rely on this compound for its reliability and effectiveness in producing complex, bioactive molecules. Its application is widespread in both basic and applied research, supporting advancements in chemical sciences and related fields.
- Asymmetric synthesis is a key application where this compound is used to create enantiomerically pure compounds, essential for pharmaceutical development.
- Chiral auxiliary applications benefit from its structural symmetry, allowing for controlled stereochemical outcomes in complex molecule synthesis.
- Organic chemistry research utilizes this compound for its stability and reactivity, supporting a wide range of synthetic pathways.
- Drug development projects rely on its ability to produce molecules with specific spatial configurations, crucial for biological activity.
- Academic research in Indonesian universities employs it for teaching and experimental purposes, enhancing understanding of stereochemistry and synthetic methods.
| Brand | TCI |
|---|---|
| CAS number | 65376-05-8 |
| Molecular formula | — |
| Purity | — |
| Category | Chemistry > Asymmetric Synthesis > Chiral Building Blocks |
| Pack sizes | 1R,2R)-1,2-Cyclohexanedimethanol |
| Physical form | Solid or liquid, depending on the specific product formulation |
| Storage | Store in a cool, dry place away from light and moisture |
This compound should be stored in a cool, dry environment, away from direct sunlight and moisture. It is recommended to use airtight containers to prevent exposure to air and humidity, which could affect its stability. Due to its chemical nature, it should be handled with appropriate personal protective equipment, including gloves and safety goggles. In laboratory settings, it should be stored separately from incompatible substances to avoid any potential chemical reactions. Regular inspection of storage conditions is advised to ensure the integrity of the compound remains intact. Proper labeling and documentation are essential for safe handling and use in research environments.
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