(1S,4S)-2-Methyl-2,5-diazabicyclo[2.2.1]heptane dihydrobromide
97%
- Product Code: 113044
CAS:
125224-62-6
| Molecular Weight: | 274 g./mol | Molecular Formula: | C₆H₁₄Br₂N₂ |
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| EC Number: | MDL Number: | ||
| Melting Point: | 220-225°C | Boiling Point: | |
| Density: | Storage Condition: | 2-8°C |
Product Description:
(1S,4S)-2-Methyl-2,5-diazabicyclo[2.2.1]heptane dihydrobromide is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of various pharmaceutical compounds. Its bicyclic structure and nitrogen-containing framework make it a valuable building block for developing drugs that target the central nervous system. Specifically, it has been explored in the creation of compounds with potential applications in treating neurological disorders, such as Parkinson's disease and Alzheimer's disease, due to its ability to interact with neurotransmitter systems. Additionally, this chemical is investigated for its role in developing ligands for nicotinic acetylcholine receptors, which are critical in modulating cognitive and behavioral functions. Its stereochemistry also allows for the production of enantiomerically pure compounds, enhancing the specificity and efficacy of resulting drugs.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.050 | 10-20 days | ฿2,120.00 |
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| 0.250 | 10-20 days | ฿5,780.00 |
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| 1.000 | 10-20 days | ฿11,550.00 |
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(1S,4S)-2-Methyl-2,5-diazabicyclo[2.2.1]heptane dihydrobromide
(1S,4S)-2-Methyl-2,5-diazabicyclo[2.2.1]heptane dihydrobromide is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of various pharmaceutical compounds. Its bicyclic structure and nitrogen-containing framework make it a valuable building block for developing drugs that target the central nervous system. Specifically, it has been explored in the creation of compounds with potential applications in treating neurological disorders, such as Parkinson's disease and Alzheimer's disease, due to its ability to interact with neurotransmitter systems. Additionally, this chemical is investigated for its role in developing ligands for nicotinic acetylcholine receptors, which are critical in modulating cognitive and behavioral functions. Its stereochemistry also allows for the production of enantiomerically pure compounds, enhancing the specificity and efficacy of resulting drugs.
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