(1R,2R,3R,5S)-(-)-IsopinocaMpheylaMine
95%
- Product Code: 36207
CAS:
69460-11-3
| Molecular Weight: | 153.26 g./mol | Molecular Formula: | C₁₀H₁₉N |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00192238 | |
| Melting Point: | 250℃ | Boiling Point: | 90℃18 mm Hg(lit.) |
| Density: | 0.914 g/mL at 20℃(lit.) | Storage Condition: | 2-8℃ |
Product Description:
(1R,2R,3R,5S)-(-)-Isopinocampheylamine is primarily used in the field of asymmetric synthesis and chiral chemistry. It serves as a chiral building block or ligand in the preparation of enantiomerically pure compounds, which are crucial in the development of pharmaceuticals, agrochemicals, and fine chemicals. Its rigid bicyclic structure and defined stereochemistry make it valuable for inducing stereoselectivity in catalytic reactions, such as hydrogenation, hydroformylation, and other transition metal-catalyzed processes. Additionally, it is employed in the synthesis of complex natural products and bioactive molecules, where precise control over stereochemistry is essential for achieving desired biological activity. Its applications also extend to the development of chiral catalysts and resolving agents for the separation of racemic mixtures.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | Colorless to Light Yellow Liquid |
| PURITY | 94.5-100 |
| Refractive index at 20 C | 1.478-1.482 |
| SPECIFIC OPTICAL ROTATIONNEAT | -44.0--38.0 |
| Infrared spectrum | Conforms to Structure |
| NMR | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿2,860.00 |
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(1R,2R,3R,5S)-(-)-IsopinocaMpheylaMine
(1R,2R,3R,5S)-(-)-Isopinocampheylamine is primarily used in the field of asymmetric synthesis and chiral chemistry. It serves as a chiral building block or ligand in the preparation of enantiomerically pure compounds, which are crucial in the development of pharmaceuticals, agrochemicals, and fine chemicals. Its rigid bicyclic structure and defined stereochemistry make it valuable for inducing stereoselectivity in catalytic reactions, such as hydrogenation, hydroformylation, and other transition metal-catalyzed processes. Additionally, it is employed in the synthesis of complex natural products and bioactive molecules, where precise control over stereochemistry is essential for achieving desired biological activity. Its applications also extend to the development of chiral catalysts and resolving agents for the separation of racemic mixtures.
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