| CAS # | 824395-67-7 |
| SMILES | |
| Chemical Purity | |
| Molecular Formula | (C16H16)PCH2CH2P(C16H16) |
| Chemical Formula | |
| Formula Weight | 506.60 |
| Reaction | |
| Note |
$1,140.00
Available on backorder. No lead time available. Please request a quote.
Sku SC15-0474_2_G
US-Strem
General Details
Physical Properties
| Purity | min. 98% |
| Density | |
| Melting Point | |
| Boiling Point | |
| Flash Point | |
| Vapor Pressure | |
| Surface Area | |
| Pore Volume | |
| Specific Rotation |
Shipping & Stability
| Safety | Yes |
| Store Cold | |
| Dry Ice | |
| Alternative Product for Air Shipment | |
| Export Limitations | |
| Pyrophoric | |
| Hygroscopic | |
| Air Sensitive | |
| Light Sensitive | |
| Heat Sensitive | |
| Moisture Sensitive | |
| Odorous Material |
Technical Notes:
1. Phenyl-BPE exhibits enhanced activity and selectivity over existing members of the BPE ligand family in rhodium catalysed asymmetric
2.This ligand is highly efficient for the hydrogenation of N-acyl aryl- enamides.
3.Molar substrate/catalyst ratios of up to 100,000/1 are achieved with excellent reactivity and enantioselectivity using
4.Ligand in the rhodium- catalyzed asymmetric hydroformylayion of thioamides
5.Ligand for asymmetric addition of allyl cyanide to kstones
6. Ligand for catalytic enantio- and diastereoselective aldol reaction of thioamides.
7- Organocatalytic 3+2 cycloaddition.
8. Site selective allenylation.
9 Asymmetric Phophonate addition.
10. Hydroboration of enamines.
