(3R,4S)-3-Hydroxy-4-phenyl-2-azetidinone is a chiral building block widely used in asymmetric synthesis to create compounds with specific stereochemistry. This compound plays a crucial role in organic chemistry laboratories, particularly in the development of bioactive molecules. Its unique molecular structure, featuring both hydroxyl and phenyl groups, allows for versatile chemical reactions and functional group modifications. As a key intermediate, it supports the synthesis of complex molecules requiring precise stereocontrol, making it an essential tool for researchers in medicinal chemistry and pharmaceutical development.
The compound’s stability and reactivity make it a preferred choice for synthetic chemists. Its ability to participate in various reaction mechanisms, such as nucleophilic substitution and ring-opening reactions, enhances its utility in the laboratory. The 3R,4S configuration ensures that the resulting products maintain the desired stereochemistry, which is vital for pharmaceutical applications where biological activity depends on molecular structure. This makes it a reliable and efficient reagent for advanced synthetic pathways.
In Indonesian laboratories, this compound is commonly used in organic chemistry research, especially in pharmacological studies and the synthesis of bioactive compounds. Its application is widespread in academic and industrial settings focused on developing new drugs and therapeutic agents. The compound’s versatility and specificity make it a valuable resource for researchers aiming to achieve precise stereochemical control in their experiments.
Related TCI products
- TCI A1124 76855-69-1 (3R,4R)-4-Acetoxy-3-[(R)-(tert-butyldimethylsilyloxy)ethyl]-2-azetidinone
- TCI C2832 160982-16-1 (S)-6-Chloro-4-hydroxy-3,4-dihydro-2H-thieno[3,2-e][1,2]thiazine 1,1-Dioxide
- TCI B3662 61478-26-0 (2S,4R)-1-(tert-Butoxycarbonyl)-4-hydroxy-2-(hydroxymethyl)pyrrolidine
- TCI H1368 68108-18-9 (S)-(-)-4-Hydroxy-2-pyrrolidone
- TCI H1200 253129-03-2 (3R,4R)-1-Benzyl-4-hydroxy-3-pyrrolidinemethanol
- TCI H0933 48172-10-7 (S)-(+)-2-Hydroxy-4-phthalimidobutyric Acid
- Asymmetric synthesis in pharmaceutical research due to its chiral configuration and reactivity.
- Organic chemistry experiments requiring precise stereocontrol for drug molecule development.
- Synthesis of bioactive compounds in medicinal chemistry laboratories.
- Research into novel drug candidates with specific stereochemical requirements.
- Development of complex organic molecules in academic and industrial settings.
| Brand | TCI |
|---|---|
| CAS number | 132127-34-5 |
| Molecular formula | — |
| Purity | — |
| Category | Chemistry > Asymmetric Synthesis > Chiral Building Blocks |
| Pack sizes | Available in various quantities as per supplier specifications |
| Physical form | Solid (exact form may vary based on supplier) |
| 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 light and moisture to maintain its chemical integrity. It is recommended to use airtight containers to prevent exposure to air and humidity, which may affect its stability. In laboratory settings, proper personal protective equipment (PPE) such as gloves and safety goggles should be worn when handling this material to ensure safety. It should be kept in a well-ventilated area to minimize inhalation risks. Avoid contact with incompatible substances to prevent any potential chemical reactions. Regular monitoring of storage conditions is advised to ensure the compound remains in optimal condition for use in research applications.
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(3R,4R)-4-Acetoxy-3-[(R)-(tert-butyldimethylsilyloxy)ethyl]-2-azetidinone TCI A1124
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