Methyl (S)-(-)-2-Isocyanato-3-methylbutyrate is a chiral building block used in asymmetric synthesis to construct molecules with specific stereochemical configurations. This compound plays a crucial role in the development of pharmaceuticals and organic compounds by enabling the synthesis of enantiomerically pure substances. Its chiral nature allows for the creation of isomers with distinct biological activities, making it essential in drug discovery and advanced chemical research. The compound is widely utilized in laboratories where precision and control over molecular structure are paramount.
The compound is valued for its chemical stability and reactivity, which make it suitable for a variety of synthetic reactions. Its solubility in organic solvents enhances its usability in laboratory settings, ensuring ease of handling and integration into complex synthetic protocols. The presence of an isocyanate group further adds to its versatility, allowing it to participate in multiple reaction pathways. These properties collectively make it a preferred choice for researchers aiming to achieve high levels of stereocontrol in their synthetic processes.
In Indonesian laboratories, this compound is commonly used in research related to organic chemistry and pharmaceutical development. It is particularly favored in academic and industrial settings where the synthesis of chiral compounds is required. Its availability through AMI Scientific ensures that researchers in Indonesia have access to high-quality materials necessary for cutting-edge scientific investigations.
TCI brochures (PDF)
- Chiral Building Blocks 2025-04-14 · p. 10
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- Asymmetric synthesis is a key application where this compound is used to create enantiomerically pure compounds, essential for drug development and pharmaceutical research.
- Organic chemistry research benefits from its chiral structure, enabling the synthesis of complex molecules with specific stereochemistry.
- Pharmaceutical development relies on this compound to produce compounds with targeted biological activities and improved therapeutic effects.
- Chiral building block applications require precise control over molecular structure, which this compound provides through its stereocenter.
- Synthetic chemistry experiments benefit from its reactivity and solubility, allowing for efficient participation in various reaction mechanisms.
| Brand | TCI |
|---|---|
| CAS number | 30293-86-8 |
| Molecular formula | — |
| Purity | — |
| Category | Chemistry > Asymmetric Synthesis > Chiral Building Blocks |
| Pack sizes | Available in various sizes as per supplier specifications |
| Physical form | Solid or liquid, depending on supplier packaging |
| Storage | Store in a cool, dry place away from moisture and direct sunlight |
This compound should be stored in a cool, dry environment to maintain its chemical stability and prevent degradation. It is recommended to use airtight containers to protect it from moisture and contaminants. Due to its reactivity, it should be handled with care in a well-ventilated laboratory setting. Proper personal protective equipment, such as gloves and safety goggles, should be worn during handling. Storage away from incompatible substances is essential to ensure safety. Regular monitoring of storage conditions is advised to maintain the integrity of the compound throughout its shelf life.
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