Basic information Reaction Safety Supplier Related

(2-BIPHENYL)DI-TERT-BUTYLPHOSPHINE GOLD&

Basic information Reaction Safety Supplier Related

(2-BIPHENYL)DI-TERT-BUTYLPHOSPHINE GOLD& Basic information

Product Name:
(2-BIPHENYL)DI-TERT-BUTYLPHOSPHINE GOLD&
Synonyms:
  • (2-BIPHENYL)DI-TERT-BUTYLPHOSPHINE GOLD&
  • Chloro[2-(di-t-butylphosphino)biphenyl]gold(I),99%
  • 1,1''-BIPHENYL]-2-YLBIS(T-BUTYLPHOSPHINE]CHLOROGOLD
  • (2-Biphenyl)di-tert-butylphosphine gold(I) chloride, 2-(Di-tert-butylphosphino)biphenyl gold(I) chloride, [[1,1μ-Biphenyl]-2-ylbis(t-butylphosphine]chlorogold
  • Chloro[(1,1μ-biphenyl-2-yl)di-tert-butylphosphine]gold(I)
  • Chloro[2-(di-t-butylphosphino)biphenyl]gold(I), 99%
  • (2-Biphenyl)di-tert-butylphosphine gold(I) chloride
  • 2-(Di-tert-butylphosphino)biphenyl gold(I) chloride
CAS:
854045-93-5
MF:
C20H28AuClP
MW:
531.83
Product Categories:
  • Au
  • organometallic complex
Mol File:
854045-93-5.mol
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(2-BIPHENYL)DI-TERT-BUTYLPHOSPHINE GOLD& Chemical Properties

Melting point:
237-240 °C
storage temp. 
under inert gas (nitrogen or Argon) at 2-8°C
form 
Powder
color 
white
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Safety Information

WGK Germany 
3
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(2-BIPHENYL)DI-TERT-BUTYLPHOSPHINE GOLD& Usage And Synthesis

Reaction

  1. Highly active gold catalyst for the intramolecular exohydrofunctionalization of allenes.
  2. Catalyst used for the hydroarylation of allenes.
  3. Catalyst used for the intramolecular cyclization of monopropargyl triols.
  4. Synthesis of pyrroles via a gold-catalyzed cascade reaction.
  5. Gold-catalyzed carboalkoxylations of 2-ethynylbenzyl ethers.
  6. Gold-catalyzed annulations of allenes with N-hydroxy anilines.

Uses

Gold Catalysts — 21st Century ′Gold Rush′

(2-BIPHENYL)DI-TERT-BUTYLPHOSPHINE GOLD&Supplier

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