Gold(1+) chloride-triphenylphosphine (1:1:1)

Modify Date: 2024-01-03 22:41:10

Gold(1+) chloride-triphenylphosphine (1:1:1) structure	Common Name	Gold(1+) chloride-triphenylphosphine (1:1:1)
	CAS Number	14243-64-2	Molecular Weight	494.71
	Density	N/A	Boiling Point	360ºC at 760 mmHg
	Molecular Formula	C₁₈H₁₅AuClP	Melting Point	248-249°C
	MSDS	Chinese USA	Flash Point	181.7ºC
	Symbol	GHS07	Signal Word	Warning

Use of Gold(1+) chloride-triphenylphosphine (1:1:1)

Triphenylphosphinechlorogold is a biochemical reagent that can be used as a biological material or organic compound for life science related research.

Name	Chloro(triphenylphosphine)gold(I)
Synonym	More Synonyms

Description	Triphenylphosphinechlorogold is a biochemical reagent that can be used as a biological material or organic compound for life science related research.
Related Catalog	Research Areas >> Others Signaling Pathways >> Others >> Others

Boiling Point	360ºC at 760 mmHg
Melting Point	248-249°C
Molecular Formula	C₁₈H₁₅AuClP
Molecular Weight	494.71
Flash Point	181.7ºC
Exact Mass	494.026489
PSA	13.59000
LogP	4.13180
Vapour Pressure	4.74E-05mmHg at 25°C
Storage condition	Store under Nitrogen

MSDS(Chinese)

Symbol	GHS07
Signal Word	Warning
Hazard Statements	H315-H319-H335
Precautionary Statements	P261-P305 + P351 + P338
Personal Protective Equipment	dust mask type N95 (US);Eyeshields;Gloves
Hazard Codes	Xi:Irritant;
Risk Phrases	R36/37/38
Safety Phrases	S26-S36/37/39-S37/39
RIDADR	NONH for all modes of transport

Precursor 8
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DownStream 9
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A mass spectrometric investigation of the binding of gold antiarthritic agents and the metabolite [Au(CN)2]- to human serum albumin.

J. Biol. Inorg. Chem. 11(5) , 559-70, (2006)

Electrospray ionisation (ESI) mass spectrometry was used to examine the reactions of the clinically used antiarthritic agent [Au(S2O3)2]3-, and AuPEt3Cl, a derivative of another clinically used agent ...

Development of a gold-multifaceted catalysis approach to the synthesis of highly substituted pyrroles: mechanistic insights via Huisgen cycloaddition studies.

J. Org. Chem. 78(3) , 920-34, (2013)

A novel gold-catalyzed method for the regioselective synthesis of highly substituted pyrroles directly from oximes and alkynes was developed via independent optimization of two key steps of the proces...

A powerful chiral counterion strategy for asymmetric transition metal catalysis.

Science 317 , 496-499, (2007)

Traditionally, transition metal-catalyzed enantioselective transformations rely on chiral ligands tightly bound to the metal to induce asymmetric product distributions. Here we report high enantiosele...

Phosphine, triphenyl-, gold(1+) salt, hydrochloride (1:1:1)

Gold(1+) chloride - triphenylphosphine (1:1:1)

(Triphenylphosphine)gold(I) Chloride

EINECS 238-117-6

Chloro(triphenylphosphine)gold

(Ph3P)AuCl (Triphenylphosphinegold(I) chloride

MFCD00009588

chlorogold,triphenylphosphane