Dimethylammonium dichlorotri(mu-chloro)bis(S)-(-)-5,5'-bis[di(3,5-xylyl)phosphino]-4,4'-bi-1,3-benzodioxolediruthenate(II) [NH2Me2][RuCl((S)-dm-segphos)2(mu-Cl)3]
97%
- Product Code: 71404
CAS:
944451-14-3
| Molecular Weight: | 18719 g./mol | Molecular Formula: | C₉₄H₉₆Cl₅NO₈P₄Ru₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD09753038 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature |
Product Description:
This compound is primarily utilized in asymmetric catalysis, particularly in hydrogenation reactions. Its structure, featuring a chiral ligand, makes it highly effective in producing enantiomerically pure compounds, which are crucial in the pharmaceutical industry for the synthesis of active pharmaceutical ingredients (APIs). The compound’s ability to selectively hydrogenate specific functional groups, such as ketones or alkenes, enables the production of chiral molecules with high optical purity. This is especially valuable in the development of drugs, where the biological activity often depends on the correct stereochemistry. Additionally, it is employed in fine chemical synthesis for creating complex organic molecules with high precision and efficiency.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | Light yellow to Amber to Dark green to Brown powder to crystal |
| PURITY | 96.5-100 |
| Infrared spectrum | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.200 | 10-20 days | £109.92 |
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Dimethylammonium dichlorotri(mu-chloro)bis(S)-(-)-5,5'-bis[di(3,5-xylyl)phosphino]-4,4'-bi-1,3-benzodioxolediruthenate(II) [NH2Me2][RuCl((S)-dm-segphos)2(mu-Cl)3]
This compound is primarily utilized in asymmetric catalysis, particularly in hydrogenation reactions. Its structure, featuring a chiral ligand, makes it highly effective in producing enantiomerically pure compounds, which are crucial in the pharmaceutical industry for the synthesis of active pharmaceutical ingredients (APIs). The compound’s ability to selectively hydrogenate specific functional groups, such as ketones or alkenes, enables the production of chiral molecules with high optical purity. This is especially valuable in the development of drugs, where the biological activity often depends on the correct stereochemistry. Additionally, it is employed in fine chemical synthesis for creating complex organic molecules with high precision and efficiency.
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