tBuXPhos Pd G3
ALDRICH/762229 - 98%
Synonym: tBuXPhos-Pd-G3; [(2-Di-tert-butylphosphino-2′,4′,6′-triisopropyl-1,1′-biphenyl)-2-(2′-amino-1,1′-biphenyl)] palladium(II) methanesulfonate
CAS Number: 1447963-75-8
Empirical Formula (Hill Notation): C42H58NO3PPdS
Molecular Weight: 794.37
MDL Number: MFCD22666411
Linear Formula: C42H58NO3PPdS
Product Type: Chemical
assay | 98% |
feature | generation 3 |
form | solid |
functional group | phosphine |
InChI | 1S/C29H45P.C12H10N.CH4O3S |
InChI key | SQQOHCLJPLSJGX-UHFFFAOYSA |
mp | 130-140 °C |
Quality Level | 100 |
reaction suitability | reaction type: Buchwald-Hartwig Cross Coupling Reaction |
reaction type: Heck Reaction | |
reaction type: Hiyama Coupling | |
reaction type: Negishi Coupling | |
reaction type: Sonogashira Coupling | |
reaction type: Stille Coupling | |
reaction type: Suzuki-Miyaura Coupling | |
reagent type: catalyst reaction type: Cross Couplings |
|
SMILES string | CS(=O)(=O)O[Pd]c1ccccc1-c |
Application: | tBuXPhos Pd G3 may be used to synthesize 4-cyano-7-azaindole from 4-chloro-7-azaindole by cyanation reaction. It may also be used for the α-arylation reaction of acetate esters at room temperature. For small scale and high throughput uses, product is also available as ChemBeads (931055 ) |
General description: | tBuXPhos Pd G3 is a third generation (G3) Buchwald precatalyst. It is air, moisture and thermally-stable and is highly soluble in a wide range of common organic solvents. It has long life in solutions. tBuXPhos Pd G3 is an excellent reagent for Buchwald-Hartwig cross-coupling reaction. Some of its unique features include lower catalyst loadings, shorter reaction time, efficient formation of the active catalytic species and accurate control of ligand: palladium ratio. |
Packaging: | 1, 5 g in glass bottle |
Packaging: | 250 mg in glass bottle |
RIDADR | NONH for all modes of transport |
WGK Germany | WGK 3 |
Flash Point(F) | Not applicable |
Flash Point(C) | Not applicable |
Purity | 98% |
mp | 130-140 °C |
UNSPSC | 12161600 |