9-Amino-(9-deoxy)epi-cinchonidine trihydrochloride
98%
- Product Code: 70660
CAS:
1263486-03-8
| Molecular Weight: | 402.78884 g./mol | Molecular Formula: | C₁₉H₂₆Cl₃N₃ |
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| EC Number: | MDL Number: | MFCD28016037 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C |
Product Description:
This compound is primarily utilized in the field of organic synthesis, particularly as a chiral catalyst or ligand in asymmetric reactions. Its unique structure enables it to facilitate enantioselective transformations, which are crucial in the production of pharmaceuticals and fine chemicals. It is often employed in asymmetric hydrogenation and carbon-carbon bond-forming reactions, where high enantiomeric purity is required. Additionally, its application extends to the development of novel catalytic systems for research purposes, aiding in the discovery of new synthetic pathways. Its trihydrochloride form enhances solubility in aqueous or polar solvents, making it more versatile in various reaction conditions.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
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| 0.010 | 10-20 days | $100.60 |
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| 0.050 | 10-20 days | $399.85 |
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9-Amino-(9-deoxy)epi-cinchonidine trihydrochloride
This compound is primarily utilized in the field of organic synthesis, particularly as a chiral catalyst or ligand in asymmetric reactions. Its unique structure enables it to facilitate enantioselective transformations, which are crucial in the production of pharmaceuticals and fine chemicals. It is often employed in asymmetric hydrogenation and carbon-carbon bond-forming reactions, where high enantiomeric purity is required. Additionally, its application extends to the development of novel catalytic systems for research purposes, aiding in the discovery of new synthetic pathways. Its trihydrochloride form enhances solubility in aqueous or polar solvents, making it more versatile in various reaction conditions.
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