(S)-(-)-2-Acetoxypropionyl Chloride is a chiral chemical compound used in asymmetric synthesis to construct complex molecular structures. It plays a crucial role in laboratories where precise control over stereochemistry is required. This compound is commonly employed in chemical reactions that demand high specificity, such as the production of pharmaceuticals or bioactive organic compounds. In the laboratory, it serves as a key building block in synthetic processes that require accuracy and reproducibility. Its chiral nature allows it to participate in asymmetric reactions, yielding products with defined stereochemical configurations. The compound's high purity and reactivity make it a preferred choice for organic chemists. Its versatility in various chemical reactions, including nucleophilic and substitution reactions, enhances its utility in diverse synthetic applications.
The compound's chiral structure and high purity contribute to its effectiveness in asymmetric synthesis. Its reactivity ensures that it can efficiently participate in a wide range of chemical transformations. The ability to produce stereospecific products makes it particularly valuable in the development of pharmaceuticals and other bioactive compounds. Its stability under controlled conditions further supports its use in laboratory settings where precision is essential. The compound's compatibility with various reaction conditions and reagents adds to its appeal for researchers working in organic chemistry. These properties collectively make it a reliable and versatile tool for synthetic chemists.
In Indonesian laboratories, this compound is used in research focused on organic synthesis and pharmaceutical development. It is commonly found in academic and industrial settings where asymmetric reactions are required. Its application supports the creation of complex molecules with specific stereochemical properties. The compound is essential for studies involving chiral building blocks and is widely utilized in both teaching and research environments. Its presence in Indonesian laboratories underscores its importance in advancing chemical research and innovation.
TCI brochures (PDF)
- Chiral Building Blocks 2025-04-14 · p. 14
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- Asymmetric Synthesis: This compound is ideal for asymmetric reactions due to its chiral structure, enabling the production of stereospecific products.
- Pharmaceutical Development: It is used in the synthesis of bioactive compounds, supporting the creation of new drug candidates with defined stereochemistry.
- Organic Chemistry Research: Its reactivity and purity make it a preferred choice for complex molecular synthesis in academic and industrial research.
- Chiral Building Block Applications: It serves as a key component in the construction of chiral molecules, essential for creating compounds with specific biological activities.
- Nucleophilic Reaction Studies: Its ability to participate in nucleophilic reactions makes it valuable for studying reaction mechanisms and stereochemical outcomes.
| Brand | TCI |
|---|---|
| CAS number | 36394-75-9 |
| Molecular formula | — |
| Purity | — |
| Category | Chemistry > Asymmetric Synthesis > Chiral Building Blocks |
| Pack sizes | Available in various quantities as per standard chemical supply practices |
| Physical form | Liquid |
| Storage | Store in a cool, dry place away from light and moisture |
This compound should be stored in a cool, dry place away from light and moisture to maintain its stability and reactivity. It is recommended to use airtight containers made of glass or high-density polyethylene to prevent contamination and degradation. Proper labeling of containers is essential to ensure safe handling and prevent accidental exposure. In laboratory settings, it should be handled with appropriate personal protective equipment, such as gloves and safety goggles. Due to its chemical nature, it should be stored separately from incompatible substances to avoid any potential reactions. Regular monitoring of storage conditions is advised to ensure the compound remains in optimal condition for use.
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