| Identification | Back Directory | [Name]
DI-TERT-BUTYLMETHYLPHOSPHONIUM TETRAFLUOROBORATE | [CAS]
479094-62-7 | [Synonyms]
DI-T-BUTYLMETHYLPHOSPHONIUM TETRAFLUOROBORATE
DI-TERT-BUTYLMETHYLPHOSPHONIUM TETRAFLUOROBORATE
Di-tert-butylmethylphosphonium tetrafluoroborate,99%
Di-tert-B-butylmethylphosphonium tetrafluoroborate, 99%
Bis(1,1-dimethylethyl)(methyl)phosphine tetrafluoroborate
Di-tert-butyl(methyl)phosphonium Tetrafluoroborate | [Molecular Formula]
C9H22BF4P | [MDL Number]
MFCD03840579 | [MOL File]
479094-62-7.mol | [Molecular Weight]
248.05 |
| Chemical Properties | Back Directory | [Appearance]
White crystalline powder | [Melting point ]
>230 °C(lit.)
| [storage temp. ]
Inert atmosphere,Room Temperature | [form ]
solid | [PH]
1.79 (1% in solution) | [InChI]
InChI=1S/C9H21P.BF4/c1-8(2,3)10(7)9(4,5)6;2-1(3,4)5/h1-7H3;/q;-1/p+1 | [InChIKey]
BRDLRXCAHKUWJS-UHFFFAOYSA-O | [SMILES]
[PH+](C)(C(C)(C)C)C(C)(C)C.[B-](F)(F)(F)F |
| Hazard Information | Back Directory | [Chemical Properties]
White crystalline powder | [Uses]
Di-tert-butyl(methyl)phosphonium tetrafluoroborate may be used in the preparation of a precursor for nantenine analogs bearing a C4 phenyl substituent, which shows an affinity for 5-HT2B receptor. It may also be used in the palladium-catalyzed borylation of primary alkyl electrophiles (bromides, iodides or tosylates) using bis(pinacolato)diboron or bis(neopentyl glycolato)diboron as the boron source. | [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 |
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