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Di-tert-butylmethylphosphine

ALDRICH/642629 - 97%

Synonym: (t-Bu)2PMe; Bis(tert-butyl)methylphosphine

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

Catalog Number PKG Qty. Price Quantity
45-642629-5G 5 g
$404.00
1/EA
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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(4,5)6/h1-7H3
InChI key JURBTQKVGNFPRJ-UHFFFAOYSA-N
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
Purity 97%
bp 58 °C/12 mmHg (lit.)
Density 0.824 g/mL at 25 °C (lit.)
UNSPSC 12352001

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