(R)-(-)-1-[(S)-2-Diphenylphosphino)ferrocenyl]ethyldicyclohexylphosphine
97%
- Product Code: 70251
Alias:
(R)-(-)-1-[(S)-2-diphenylphosphonium]ferrocenylethyldicyclohexylphosphonium; (R)-1-1[(S)-2-(diphenylphosphonium Phosphin)ferrocene]ethyldicyclohexylphosphine;(2R)-1-[(1R)-1-(dicyclohexylphosphino)ethyl]-2-diphenylphosphinoferrocene;( R)-1-[(S)-2-(diphenylphosphino)ferrocenyl]-ethyl-dicyclohexylphosphine ethanol adduct; (R)-1-[(S)-2- (Diphenylphosphino)ferrocenyl]-ethyl-dicyclohexylphosphine ethanol adduct, manufactured by SOLVIAS AG; (R)-(-)-1-[(S)-2-Diphenylphosphine ]Ferroceneethyldicyclohexylphosphine; (2R)-1-[(1R)-1-(dicyclohexylphosphine)
CAS:
155806-35-2
| Molecular Weight: | 594.53 g./mol | Molecular Formula: | C₃₆H₄₄FeP₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00800284 | |
| Melting Point: | -95ºC (dec.) | Boiling Point: | |
| Density: | Storage Condition: | room temperature |
Product Description:
This chemical is widely used as a chiral ligand in asymmetric catalysis, particularly in hydrogenation reactions. It facilitates the production of enantiomerically pure compounds, which are crucial in the pharmaceutical industry for synthesizing active pharmaceutical ingredients (APIs) with high stereoselectivity. Its application extends to the synthesis of fine chemicals and agrochemicals, where precise control over molecular chirality is essential. Additionally, it is employed in academic research to develop and optimize new catalytic processes, contributing to advancements in organic synthesis and material science.
Product Specification:
| Test | Specification |
|---|---|
| Purity | 96.5 100% |
| Appearance | Orange Crystal or Powder |
| Infrared spectrum | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿750.00 |
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| 0.250 | 10-20 days | ฿1,760.00 |
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| 1.000 | 10-20 days | ฿2,800.00 |
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(R)-(-)-1-[(S)-2-Diphenylphosphino)ferrocenyl]ethyldicyclohexylphosphine
This chemical is widely used as a chiral ligand in asymmetric catalysis, particularly in hydrogenation reactions. It facilitates the production of enantiomerically pure compounds, which are crucial in the pharmaceutical industry for synthesizing active pharmaceutical ingredients (APIs) with high stereoselectivity. Its application extends to the synthesis of fine chemicals and agrochemicals, where precise control over molecular chirality is essential. Additionally, it is employed in academic research to develop and optimize new catalytic processes, contributing to advancements in organic synthesis and material science.
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