(S)-(+)-2-Phenylpropionic Acid is a chiral compound widely used in asymmetric synthesis to construct molecules with specific biological activities. This material plays a crucial role in organic chemistry laboratories, particularly in the development of pharmaceuticals and other chiral compounds. Its unique stereochemistry allows for the creation of enantiomerically pure substances, which are essential in drug discovery and development. As a chiral building block, it provides a foundation for synthesizing complex molecules with precise stereochemical control.
The compound’s molecular structure, featuring a phenyl group and a carboxylic acid group, gives it reactivity and polarity that make it ideal for various chemical reactions. These properties enable it to participate in esterification, hydrolysis, and asymmetric reactions requiring enantiospecific substrates. Its chiral nature also allows researchers to produce compounds with distinct biological activities depending on the enantiomer formed. This makes it a valuable tool for studying the effects of stereochemistry on molecular function.
In Indonesian laboratories, (S)-(+)-2-Phenylpropionic Acid is commonly used by chemists and pharmacologists for the development of new compounds, biological activity testing, and research into stereochiral effects. It is an essential component in studies that require precise control over molecular structure and stereochemistry. Its versatility and reliability make it a preferred choice for both academic and industrial research settings.
TCI brochures (PDF)
- Chiral Auxiliaries and Optical Resolving Agents 2025-06-17 · p. 6
- Chiral Building Blocks 2025-04-14 · p. 13
Related TCI products
- TCI P1219 7782-26-5 (R)-(-)-2-Phenylpropionic Acid
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- TCI T1520 53531-34-3 (R)-(-)-2,2,2-Trifluoro-1-(9-anthryl)ethanol [e.e. Determination Reagent by NMR]
- TCI B1144 35193-64-7 (S)-(+)-1,1'-Binaphthyl-2,2'-diyl Hydrogen Phosphate
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- Asymmetric synthesis applications benefit from its chiral structure, enabling the creation of enantiomerically pure compounds for pharmaceutical development.
- Organic chemistry research utilizes its reactivity and polarity for esterification and hydrolysis reactions in compound synthesis.
- Pharmaceutical development relies on its ability to produce compounds with specific biological activities through enantiospecific reactions.
- Stereochemical studies use it to investigate the impact of molecular chirality on biological activity and molecular interactions.
- Drug discovery projects incorporate it as a key building block for designing molecules with targeted pharmacological effects.
| Brand | TCI |
|---|---|
| CAS number | 7782-24-3 |
| Molecular formula | — |
| Purity | — |
| Category | Chemistry > Asymmetric Synthesis > Chiral Building Blocks |
| Pack sizes | Available in standard laboratory quantities |
| Physical form | Solid |
| 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 maintain its chemical integrity. Due to its chiral nature, it is important to handle it with care to avoid contamination or cross-contamination with other substances. Proper labeling of containers is essential to ensure safe handling and accurate identification. In laboratory settings, it should be stored in a designated chemical storage area that complies with safety regulations. Always use appropriate personal protective equipment when handling this material to ensure safety and compliance with laboratory protocols.
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