(S)-1-(Diphenylphosphino)-2-[(S)-4-isopropyloxazolin-2-yl]ferrocene
97%
- Product Code: 69734
Alias:
(S)[(Sp)-2-(diphenylphosphino)ferrocenyl]-4-isopropyloxazoline(Sp)-1-(diphenylphosphine)-2-[(4S)- 4-Isopropyl-2-oxazolyl]ferrocene
CAS:
163169-29-7
| Molecular Weight: | 481.36 g./mol | Molecular Formula: | C₂₈H₂₈FeNOP |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD15144869 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature |
Product Description:
This chemical is primarily used as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions. It is highly effective in enantioselective transformations, such as hydrogenation, coupling reactions, and carbon-carbon bond-forming processes. Its unique structure, combining a ferrocene backbone with phosphine and oxazoline groups, provides excellent steric and electronic control, enabling the production of chiral compounds with high enantiomeric purity. This makes it valuable in the synthesis of pharmaceuticals, agrochemicals, and fine chemicals where precise stereochemistry is crucial. Additionally, its stability and versatility allow it to be used in a wide range of reaction conditions, making it a preferred choice in organic synthesis.
Product Specification:
| Test | Specification |
|---|---|
| CARBON | 67.4 72.3% |
| Melting point | 157 162? |
| PURITYCHELOMETRIC TITRATION | 95.5-100 |
| PurityGC | 95.5 100% |
| SPECIFIC ROTATION A20DC 0.1 CHCL3 | 330-403 |
| APPEARANCE | Yellow to brown powder or crystals |
| INFRARED SPECTROMETRY | Conforms to Structure |
| PROTON NMR SPECTRUM | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿1,290.00 |
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| 0.250 | 10-20 days | ฿2,600.00 |
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(S)-1-(Diphenylphosphino)-2-[(S)-4-isopropyloxazolin-2-yl]ferrocene
This chemical is primarily used as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions. It is highly effective in enantioselective transformations, such as hydrogenation, coupling reactions, and carbon-carbon bond-forming processes. Its unique structure, combining a ferrocene backbone with phosphine and oxazoline groups, provides excellent steric and electronic control, enabling the production of chiral compounds with high enantiomeric purity. This makes it valuable in the synthesis of pharmaceuticals, agrochemicals, and fine chemicals where precise stereochemistry is crucial. Additionally, its stability and versatility allow it to be used in a wide range of reaction conditions, making it a preferred choice in organic synthesis.
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