(R)-2,3-Dihydro-1H-inden-1-ol is a chiral building block used in asymmetric synthesis to construct molecules with specific biological activities. This compound plays a vital role in laboratories where the development of optically active compounds is essential. Its chiral nature allows for precise control over the stereochemistry of synthesized products, making it a key component in advanced chemical research. It is widely applied in the creation of pharmaceuticals and bioactive molecules, supporting the development of new therapeutic agents.
The compound's structural features, including its indene framework, contribute to its stability and reactivity under various reaction conditions. These characteristics make it a preferred choice for chemists working on complex molecular transformations. Its ability to participate in enantioselective reactions enhances its utility in the synthesis of compounds with defined stereochemistry. The compound's chiral properties are particularly valuable in the field of organic chemistry and pharmacology.
In Indonesian laboratories, (R)-2,3-Dihydro-1H-inden-1-ol is commonly used in research focused on bioactive compounds, especially in pharmaceutical and biochemical studies. Its availability supports local researchers in conducting experiments that require chiral intermediates. The compound is essential for developing new drugs and understanding the stereochemical effects on biological activity. Its use is widespread in academic and industrial research settings across Indonesia.
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- Asymmetric Synthesis: This compound is ideal for creating optically active molecules due to its chiral structure, enabling precise control over stereochemistry in complex reactions.
- Pharmaceutical Research: It is used in the development of new drugs, supporting the synthesis of compounds with specific biological activities and therapeutic potential.
- Organic Chemistry Studies: Its reactivity and stability make it a valuable tool for exploring molecular transformations and reaction mechanisms in organic synthesis.
- Bioactive Compound Development: Researchers use it to design and test compounds with potential applications in medicine and biotechnology.
- Stereochemical Analysis: The compound's chiral nature aids in studying the effects of stereochemistry on molecular behavior and biological interactions.
| Brand | TCI |
|---|---|
| CAS number | 697-64-3 |
| Molecular formula | — |
| Purity | — |
| Category | Chemistry > Asymmetric Synthesis > Chiral Building Blocks |
| Pack sizes | Available in various quantities as per standard laboratory supply |
| Physical form | Solid (as per standard product description) |
| Storage | Store in a cool, dry place away from light |
This compound should be stored in a cool, dry environment, away from direct sunlight and sources of heat. It is recommended to use airtight containers to prevent moisture absorption and contamination. Proper labeling of storage containers is essential for safety and traceability. Due to its chiral nature, it is important to maintain the integrity of the compound during handling to ensure the accuracy of experimental results. Laboratory personnel should wear appropriate personal protective equipment when handling the material to ensure safety. The compound should be kept in a secure location to prevent unauthorized access and ensure compliance with laboratory safety protocols.
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