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Merck

665185

Bis(chlorogold(I)) bis(diphenylphosphino)methane

97%, solid

Sustainability features

Synonym(s):

Methylenebis[diphenyl]phosphine gold complex

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About This Item

Empirical Formula (Hill Notation):
C25H22Au2Cl2P2
CAS Number:
Molecular Weight:
849.23
UNSPSC Code:
12161600
PubChem Substance ID:
NACRES:
NA.22
MDL number:
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Product Name

Bis(chlorogold(I)) bis(diphenylphosphino)methane, 97%

Quality Segment

assay

97%

form

solid

reaction suitability

core: gold, reagent type: catalyst

greener alternative product characteristics

Catalysis
Learn more about the Principles of Green Chemistry.

sustainability

Sustainability features

greener alternative category

SMILES string

Cl[Au][PH](C[PH]([Au]Cl)(c1ccccc1)c2ccccc2)(c3ccccc3)c4ccccc4

InChI

1S/C25H22P2.2Au.2ClH/c1-5-13-22(14-6-1)26(23-15-7-2-8-16-23)21-27(24-17-9-3-10-18-24)25-19-11-4-12-20-25;;;;/h1-20H,21H2;;;2*1H/q;2*+1;;/p-2

InChI key

JNPUWTQJFLJEJC-UHFFFAOYSA-L

General description

We are committed to bringing you Greener Alternative Products, which adhere to one or more of the 12 Principles of Green Chemistry. This catalyst enables alkyne activation, cyclization, and C-H functionalization under mild conditions. Its superior selectivity enables elegant synthetic routes to complex heterocycles, reducing step count and waste. Click here for more information.

Application

Used for
  • Pharmacological studies involving the anticancer activity of gold(I)-phosphine complexes as autophagy-inducing agents
  • Triplet luminescent light emitting diodes with low turn-on voltage

Catalyst for:
  • Stereoselective preparation of vinyltetrahydrofuran via intramolecular hydroalkoxylation
  • Hydroamination and hydroalkoxylation reactions
  • Asymmetric transition metal catalysis
  • Gold(I) catalyzed intramolecular Schmidt reactions of homopropargyl azides


Storage Class

11 - Combustible Solids

WGK

WGK 3

Flash Point (°F)

Not applicable

Flash Point (°C)

Not applicable

PPE (personal protective equipment)

Eyeshields, Gloves, type N95 (US)



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