(3 paragraphs. Paragraph 1 AT LEAST 70 words: what this material/instrument is and its role in the laboratory. Paragraph 2 AT LEAST 70 words: the properties that make it a preferred choice. Paragraph 3 AT LEAST 60 words: typical use context in Indonesian laboratories.)
(TCI I1089 150529-94-5, (R,R)-2,2'-Isopropylidenebis(4-isopropyl-2-oxazoline), is a chiral reagent widely used in asymmetric synthesis. This compound plays a crucial role in the laboratory by enabling the selective synthesis of enantiomerically pure compounds. Its application is particularly important in the development of pharmaceuticals and other complex molecules where stereochemistry significantly affects the final product's properties. In research settings, it is a key component for achieving high enantiomeric excess and is essential for studies involving chiral catalysis and ligand-based reactions.
The compound is valued for its high chiral purity and its ability to act as an efficient chiral reagent in various synthetic pathways. Its molecular structure allows for effective interaction with transition metal catalysts, enhancing reaction selectivity and yield. The compound is also known for its stability under a range of reaction conditions, making it a reliable choice for both academic and industrial research. These properties make it a preferred option for chemists working in the field of asymmetric synthesis and chiral chemistry.
In Indonesian laboratories, this compound is commonly used in pharmaceutical research and organic chemistry studies. It supports the development of new drugs and the investigation of complex chemical reactions. Its availability through AMI Scientific ensures that researchers in Indonesia can access high-quality chiral reagents for their experiments and projects.
TCI brochures (PDF)
- Chiral Ligands 2024-12-13 · p. 3
- Ligands 2025-12-01 · p. 3
Related TCI products
- TCI I1051 131833-92-6 (S,S)-2,2'-Isopropylidenebis(4-isopropyl-2-oxazoline)
- TCI I0795 131833-97-1 (R,R)-(+)-2,2'-Isopropylidenebis(4-tert-butyl-2-oxazoline)
- TCI I0582 131457-46-0 (S,S)-2,2'-Isopropylidenebis(4-phenyl-2-oxazoline)
- TCI I0567 131833-93-7 (S,S)-(-)-2,2'-Isopropylidenebis(4-tert-butyl-2-oxazoline)
- TCI D2823 150529-93-4 (R,R)-2,2'-Isopropylidenebis(4-phenyl-2-oxazoline)
- TCI B4196 929896-22-0 (S,S)-4,6-Bis(4-isopropyl-2-oxazolin-2-yl)-m-xylene
- Asymmetric Synthesis: This compound is ideal for asymmetric synthesis due to its chiral structure, enabling the production of enantiomerically pure compounds essential for pharmaceutical development.
- Chiral Catalyst Research: It is frequently used in studies involving chiral catalysts, where its ability to influence reaction pathways is critical for achieving desired stereochemical outcomes.
- Organic Chemistry Studies: Its application in organic chemistry allows for the exploration of reaction mechanisms and reactivity, supporting both fundamental and applied research.
- Drug Development: It is a valuable tool in the development of new drugs, where stereochemistry plays a key role in determining the efficacy and safety of the final product.
- Academic Research: It is widely used in academic institutions for teaching and research, providing students and researchers with a reliable chiral reagent for experimental work.
| Brand | TCI |
|---|---|
| CAS number | 150529-94-5 |
| Molecular formula | — |
| Purity | — |
| Category | Chemistry > Asymmetric Synthesis > Chiral Catalysts, Chiral Ligands, Chiral Reagents |
| Pack sizes | Available in various quantities as per supplier specifications |
| Physical form | Solid, crystalline |
| 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 sunlight and sources of moisture. It is recommended to use airtight containers to prevent exposure to air and humidity, which may affect its stability. Proper labeling of containers is essential to ensure safe handling and prevent accidental contamination. In laboratory settings, it is important to use appropriate personal protective equipment when handling the compound. Due to its chiral nature, it should be handled with care to maintain its integrity during synthesis and storage. Always follow standard laboratory safety protocols to ensure safe usage and preservation of the compound's properties.
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