(R)-(-)-2,2-Dimethyl-1,3-dioxolane-4-methanol is a chiral building block widely used in asymmetric synthesis to construct molecules with optical activity. This compound plays a crucial role in organic chemistry laboratories, particularly in the development of bioactive compounds. Its chiral nature allows for the selective synthesis of enantiomers, which are essential in pharmaceutical and biochemical research. As a key component in the creation of optically active molecules, it supports the design of compounds with specific biological functions.
The compound's stable dioxolane ring structure and good solubility in organic solvents make it a preferred choice for synthetic chemists. These properties ensure that it remains chemically inert during reactions, minimizing unwanted side reactions. Its optical activity enables precise control over isomer selection and separation, which is vital for producing pharmaceuticals with high enantiomeric purity. This makes it an essential tool for researchers aiming to develop therapeutically relevant compounds.
In Indonesian laboratories, this compound is commonly used in applied research within the fields of pharmacy, biochemistry, and organic chemistry. It is a foundational material for experiments aimed at creating new compounds with potential medical or industrial applications. Many research institutions and universities rely on it for the synthesis of optically active substances, contributing to advancements in drug development and chemical innovation.
TCI brochures (PDF)
- Chiral Building Blocks 2025-04-14 · p. 15
Related TCI products
- TCI B2137 16495-03-7 (S)-4-Benzyloxymethyl-2,2-dimethyl-1,3-dioxolane
- TCI B2136 14347-83-2 (R)-4-Benzyloxymethyl-2,2-dimethyl-1,3-dioxolane
- TCI H1189 32233-43-5 (S)-4-(2-Hydroxyethyl)-2,2-dimethyl-1,3-dioxolane
- TCI H1188 70005-89-9 (R)-4-(2-Hydroxyethyl)-2,2-dimethyl-1,3-dioxolane
- TCI D2562 52373-72-5 Methyl (R)-(+)-2,2-Dimethyl-1,3-dioxolane-4-carboxylate
- TCI D1691 22323-82-6 (S)-(+)-2,2-Dimethyl-1,3-dioxolane-4-methanol
- Asymmetric synthesis of optically active pharmaceutical compounds due to its chiral structure and optical activity.
- Development of bioactive molecules in biochemical research requiring precise isomer control.
- Synthesis of enantiomerically pure compounds for drug discovery and medicinal chemistry applications.
- Use in organic chemistry experiments to explore stereochemical outcomes in complex reaction mechanisms.
- Support for the production of isomers with specific functional properties in industrial chemical applications.
| Brand | TCI |
|---|---|
| CAS number | 14347-78-5 |
| Molecular formula | — |
| Purity | — |
| Category | Chemistry > Asymmetric Synthesis > Chiral Building Blocks |
| Pack sizes | Available in various quantities as per standard laboratory supply formats |
| Physical form | Liquid |
| 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 stability and optical activity. It is recommended to use airtight containers made of glass or high-density polyethylene to prevent contamination and evaporation. As a chiral compound, it should be handled with care to avoid exposure to air or moisture, which may affect its purity and reactivity. Proper labeling and storage conditions are essential to ensure its effectiveness in laboratory applications. Always use appropriate personal protective equipment when handling this material to ensure safety in the laboratory setting.
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