(1S,4S)-2-Benzyl-2,5-diazabicyclo[2.2.1]heptane Dihydrobromide is a chiral compound widely used in asymmetric synthesis to construct complex molecular structures. This compound plays a crucial role in chemical laboratories, particularly in research requiring precise control over stereochemistry. Its unique structure allows for targeted chemical reactions, making it essential in the development of bioactive compounds. The compound is a key component in the synthesis of various pharmaceutical and biochemical molecules, where stereochemical purity is critical for achieving desired biological activity.
The compound’s chiral nature and cyclic structure make it a preferred choice for asymmetric reactions. Its ability to participate in nucleophilic and electrophilic reactions enhances its versatility in synthetic pathways. The dihydrobromide form provides stability and reactivity, enabling efficient synthesis of complex molecules. This compound is highly valued in research settings where controlled stereochemistry is essential for producing compounds with specific biological functions. Its reliability and effectiveness have made it a staple in modern synthetic chemistry.
In Indonesian laboratories, this compound is commonly used in chemical, pharmaceutical, and biochemical research. Scientists rely on it for developing new compounds with therapeutic potential or industrial applications. Its availability in the local market supports ongoing research efforts, ensuring that researchers can access the necessary materials for their experiments. The compound’s role in creating chiral molecules is vital for advancing scientific knowledge and innovation in these fields.
TCI brochures (PDF)
- Chiral Building Blocks 2025-04-14 · p. 5
Related TCI products
- TCI D6152 113451-59-5 tert-Butyl (1S,4S)-2,5-Diazabicyclo[2.2.1]heptane-2-carboxylate
- TCI D2658 132747-20-7 (1S,4S)-2,5-Diazabicyclo[2.2.1]heptane Dihydrobromide
- TCI D4210 151213-40-0 (1S,6S)-2,8-Diazabicyclo[430]nonane
- TCI T2902 97538-67-5 (2R,5S)-2-Trichloromethyl-3-oxa-1-azabicyclo[3.3.0]octan-4-one
- TCI D6516 869494-16-6 tert-Butyl 3,6-Diazabicyclo[3.1.1]heptane-6-carboxylate
- TCI D6478 1251017-66-9 tert-Butyl 3,6-Diazabicyclo[3.1.1]heptane-3-carboxylate
- Asymmetric Synthesis: This compound is ideal for asymmetric reactions due to its chiral structure, allowing for the selective formation of stereoisomers with high enantiomeric purity.
- Pharmaceutical Research: It is used in the development of new drugs, where precise stereochemistry is essential for biological activity and therapeutic efficacy.
- Biochemical Studies: The compound supports research into enzyme mechanisms and molecular interactions, aiding in the understanding of complex biological systems.
- Organic Chemistry Education: It serves as a valuable teaching tool for students learning about chiral synthesis and stereochemical control in laboratory settings.
- Industrial Chemical Synthesis: Its reactivity and stability make it suitable for large-scale production of chiral compounds used in various industries.
| Brand | TCI |
|---|---|
| CAS number | 116258-17-4 |
| Molecular formula | — |
| Purity | — |
| Category | Chemistry > Asymmetric Synthesis > Chiral Building Blocks |
| Pack sizes | Available in various quantities as per standard chemical supply practices |
| Physical form | Solid powder |
| 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 purity. It is recommended to use airtight containers to prevent exposure to humidity and contaminants. Due to its chiral nature, it is important to handle the compound with care to avoid any unintended stereochemical changes during synthesis. Proper labeling and storage conditions are essential to ensure the compound remains effective for its intended applications. Laboratory personnel should follow standard safety protocols when handling this material, including the use of appropriate personal protective equipment. Regular inspection of storage conditions ensures the compound remains suitable for use in research and synthesis processes.
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