Di-tert-butylmethylphosphine
ALDRICH/642629 - 97%
Synonym: (t-Bu)2PMe; Bis(tert-
CAS Number: 6002-40-0
Empirical Formula (Hill Notation): C9H21P
Molecular Weight: 160.24
MDL Number: MFCD11869304
Linear Formula: [(CH3)3C]2PCH3
Product Type: Chemical
assay | 97% |
bp | 58 °C/12 mmHg (lit.) |
density | 0.824 g/mL at 25 °C (lit.) |
functional group | phosphine |
InChI | 1S/C9H21P/c1-8(2,3)10(7)9 |
InChI key | JURBTQKVGNFPRJ-UHFFFAOYSA |
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: ligand reaction type: Cross Couplings |
|
SMILES string | CP(C(C)(C)C)C(C)(C)C |
Application: | Bulky phosphine used with various palladium complexes in cross-coupling catalysis. |
Application: | Di-tert-butylmethylphosphine (PtBu2Me) when added as HBF4 salt, enhances the reactivity of palladium-catalyzed direct arylation of heterocylic arenes with aryl chlorides, bromides and azine N-oxides with aryl triflates to form the corresponding biaryl and 2-aryl azine N-oxides, respectively. It may be used in the preparation of CoCl2(PtBu2Me)2, a cobalt phosphine complex, which in combination with methylaluminoxane (MAO) catalyzes the butadiene polymerization to form predominantly the cis-1,4 polymer. |
Packaging: | 5 g in glass bottle |
Symbol | GHS02,GHS05 |
Signal word | Danger |
Hazard statements | H250 - H314 |
Precautionary statements | P222 - P231 - P280 - P305 + P351 + P338 - P310 - P422 |
Hazard Codes | F,C |
Risk Statements | 17-34 |
Safety Statements | 16-26-36/37/39-45 |
RIDADR | UN 2845 4.2 |
WGK Germany | WGK 3 |
Flash Point(F) | Not applicable |
Flash Point(C) | Not applicable |
Purity | 97% |
bp | 58 °C/12 mmHg (lit.) |
Density | 0.824 g/mL at 25 °C (lit.) |
UNSPSC | 12352001 |