(S)-(-)-3-Amino-2-piperidone is a chiral building block widely used in asymmetric synthesis to construct complex molecular structures. This compound plays a critical role in organic chemistry laboratories, where it serves as a key intermediate in the development of bioactive molecules. Its optical activity and chiral nature make it indispensable for creating enantiomerically pure compounds, which are essential in pharmaceutical and medicinal research. As a versatile reagent, it supports various synthetic pathways, contributing to the advancement of drug discovery and chemical innovation.
The compound’s unique chemical structure and high purity make it a preferred choice for researchers requiring precision and consistency. Its ability to participate in nucleophilic and substitution reactions enhances its utility in synthetic processes. The stability of (S)-(-)-3-Amino-2-piperidone ensures reliable performance across multiple experimental conditions, making it a trusted material in both academic and industrial settings. Its chiral properties also allow for the selective synthesis of compounds with specific stereochemical configurations, which is crucial in the development of therapeutics.
In Indonesian laboratories, (S)-(-)-3-Amino-2-piperidone is commonly used in pharmacological research and the synthesis of pharmaceutical compounds. Local researchers rely on this compound to develop new therapeutic agents with targeted biological activities. Its availability in the local market ensures that it is accessible to both academic institutions and research organizations, supporting ongoing scientific advancements in the region.
TCI brochures (PDF)
- Chiral Building Blocks 2025-04-14 · p. 4
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- Asymmetric synthesis is a key application where (S)-(-)-3-Amino-2-piperidone is used to create enantiomerically pure compounds, essential for pharmaceutical development.
- Medicinal chemistry research benefits from this compound’s chiral structure, enabling the synthesis of bioactive molecules with specific stereochemistry.
- Organic synthesis experiments often employ this reagent due to its reactivity in nucleophilic and substitution reactions, supporting a wide range of chemical transformations.
- Drug discovery projects utilize this compound to develop new therapeutic agents with targeted biological activities and improved pharmacological profiles.
- Academic research in Indonesian universities frequently incorporates this material to advance studies in synthetic chemistry and pharmaceutical sciences.
| Brand | TCI |
|---|---|
| CAS number | 34294-79-6 |
| Molecular formula | — |
| Purity | — |
| Category | Chemistry > Asymmetric Synthesis > Chiral Building Blocks |
| Pack sizes | Available in various quantities as per standard laboratory supply |
| Physical form | Solid |
| Storage | Store in a cool, dry place away from light and moisture |
(S)-(-)-3-Amino-2-piperidone should be stored in a cool, dry environment to maintain its chemical stability and prevent degradation. It is recommended to keep the compound in a sealed container to minimize exposure to moisture and air. For long-term storage, a desiccator or a container with a desiccant can be used to ensure optimal conditions. The compound should be handled in a well-ventilated area to avoid inhalation of vapors. It is important to use appropriate personal protective equipment, such as gloves and safety goggles, when handling this material. Proper labeling of storage containers is essential to ensure safe access and prevent accidental exposure.
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![(R)-(-)-alpha-[[(4-Ethyl-2,3-dioxo-1-piperazinyl)carbonyl]amino]benzeneacetic Acid (CAS 63422-71-9) - TCI E0993 - AMI Scientific](http://amiscientific.com/cdn/shop/files/TCI2510E0993.jpg?v=1767112124&width=533)

