$755.00

FREE
SHIPPING

100% MONEY
BACK GUARANTEE

ONLINE
SUPPORT 24/7

Available on backorder. No lead time available. Please request a quote.
Sku SC46-3010_10_G
US-Strem
Get Bulk Quote
General Details
CAS # 52522-40-4
SMILES
Chemical Purity
Molecular Formula (C6H5CH=CHCOCH=CHC6H5)3Pd2CHCl3
Chemical Formula
Formula Weight 1035.08
Reaction
Note
Physical Properties
Purity
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.Used for Pd-catalyzed asymmetric arylation, vinylation, and Allenylation of tert-cyclobutanols via
enantioselective c-c Bond cleavage.
2.Used for synthesis of chiral chromans through the Pd-catalyzed asymmetric allylic alkylation (AAA).
4.Catalyst for double N-arylation of primary amines to synthesize multisubstituted carbazoles from 2,2'- biphenylylene ditriflates .
4. Paladium catalyst for regio- and enantioselective allylic alkylation of ketones through allyl enol carbonates .
5.Used for Pd-catalyzed enantioselective C-3 allylation of 3-substituted-1H-indoles using trialkylboranes.
6.Used for enantioselective construction of spirocyclic oxindolic cyclopentanes by Pd-catalyzed
trimethylenemethane-[3 +2]-cycloaddition.
7. Usewd for Pd-catalyzed insertion of a diazoesters into vinyl halides to generate a,ß-unsaturated Y amino
Esters.
8.Pd catalyst for decarboxylative asymmetric allylic alkylation of enol carbonates .
9.Palladium catalyst for asymmetric addition of oxindoles and allenes
10. Catalyst for diastereo- and enantioselective formal [3+ 2]-cycloaddition between substituted
vinylcyclopropanes and electron-deficient olefins.
11. Used for Pd-catalyzed asymmetric decarboxylative cycloaddition of vinylethylene carbonates with Michael
sacceptors.
12. Catalyst for enantioselective [6+4] cycloaddition of vinyl oxetanes with azadienes to access ten-membered
heterocycles.