(R,R)-DIPAMP
97%
- Product Code: 68591
Alias:
(R,R)-DIPAMP,(R,R)-Ethylene bis[(2-methoxyphenyl)phenylphosphine] (R,R)?-?1,2-?Ethanediylbis[( 2-?Methoxyphenyl)?Phenylphosphine] (R,R)?-?1,2-?Bis[(2-?Methoxyphenyl)?(phenylphosphino)?]?Ethyl Alkane[(1R,2R)?-?(-?)?-?Bis[(2-?Methoxyphenyl)?Phenylphosphine]?Ethane]
CAS:
55739-58-7
| Molecular Weight: | 458.47 g./mol | Molecular Formula: | C₂₈H₂₈O₂P₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD05863546 | |
| Melting Point: | 102-104 °C | Boiling Point: | |
| Density: | Storage Condition: | room temperature |
Product Description:
(R,R)-DIPAMP is widely used as a chiral ligand in asymmetric catalysis, particularly in hydrogenation reactions. It is highly effective in the synthesis of enantiomerically pure compounds, which are crucial in the production of pharmaceuticals. For example, it is employed in the asymmetric hydrogenation of prochiral olefins, ketones, and imines, enabling the production of chiral intermediates with high enantioselectivity. Its application is prominent in the synthesis of L-DOPA, a drug used to treat Parkinson's disease. Additionally, (R,R)-DIPAMP is utilized in the preparation of fine chemicals and agrochemicals, where precise stereocontrol is essential for achieving desired biological activity. Its robust performance and selectivity make it a valuable tool in organic synthesis and industrial processes.
Product Specification:
| Test | Specification |
|---|---|
| Melting point | 102 106? |
| PURITYHPLC | 97 100% |
| PURITYIODOMETRIC TITRATION | 96.5 103.5% |
| SPECIFIC ROTATION A20DC1 CHCL3 | 82 86 |
| APPEARANCE | WHITE TO TAN CRYSTAL OR POWDER |
| INFRARED SPECTRUM | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | $280.38 |
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| 0.250 | 10-20 days | $634.01 |
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(R,R)-DIPAMP
(R,R)-DIPAMP is widely used as a chiral ligand in asymmetric catalysis, particularly in hydrogenation reactions. It is highly effective in the synthesis of enantiomerically pure compounds, which are crucial in the production of pharmaceuticals. For example, it is employed in the asymmetric hydrogenation of prochiral olefins, ketones, and imines, enabling the production of chiral intermediates with high enantioselectivity. Its application is prominent in the synthesis of L-DOPA, a drug used to treat Parkinson's disease. Additionally, (R,R)-DIPAMP is utilized in the preparation of fine chemicals and agrochemicals, where precise stereocontrol is essential for achieving desired biological activity. Its robust performance and selectivity make it a valuable tool in organic synthesis and industrial processes.
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