[mu-Bis(diphenylphosphino)methane]dichlorodigold(III),99%
[mu-Bis(diphenylphosphino)methane]dichlorodigold(III),99% Basic information
- Product Name:
- [mu-Bis(diphenylphosphino)methane]dichlorodigold(III),99%
- Synonyms:
-
- [μ-Bis(diphenylphosphino)methane]dichlorodigold(I),98%
- (DPPM)(AuCl)2
- Bis(chlorogold) bis(diphenylphosphino)methane
- [μ-Bis(diphenylphosphino) methane]dichlorodigold(I), 99%
- [Mu-Bis(diphenylphosphino)Methane]dichlorodigold(III)
- [mu-Bis(diphenylphosphino)methane]dichlorodigold(I), 99%
- [mu-Bis(diphenylphosphino)methane]dichlorodigold(III),99%
- [Mu-Bis(diphenylphosphino)Methane]dichlorodigold(I),99%
- CAS:
- 37095-27-5
- MF:
- C25H22P2.2AuCl
- MW:
- 849.243
- Product Categories:
-
- Au
- organometallic complex
- Mol File:
- 37095-27-5.mol
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[mu-Bis(diphenylphosphino)methane]dichlorodigold(III),99% Chemical Properties
- Melting point:
- 271-272℃
- form
- Powder
- color
- white
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[mu-Bis(diphenylphosphino)methane]dichlorodigold(III),99% Usage And Synthesis
Reactions
- Catalyst used with chiral counter-ion for asymmetric hydroalkoxylation.
- Catalyst used for intramolecular acetylene Schmidt reaction.
Uses
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
[mu-Bis(diphenylphosphino)methane]dichlorodigold(III),99%Supplier
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