gold(III) chloride
Conditions | Yield |
---|---|
byproducts: SO2, SO3; in melt; |
Conditions | Yield |
---|---|
With hydrogenchloride In water heating in sealed tube, 100°C; |
gold(III) chloride
Conditions | Yield |
---|---|
With thionyl chloride In neat (no solvent) heating in sealed tube, 200°C (minimum 10 days); | |
With chlorine gaseous Cl2, at moderated temp.; | |
With chlorine gaseous Cl2, in presence of moisture, at ambient temp.; |
Conditions | Yield |
---|---|
In not given Kinetics; | |
In not given Kinetics; |
Conditions | Yield |
---|---|
In neat (no solvent) 200°C; 10 d (small yield);; | |
In neat (no solvent) 200°C; 10 d (small yield);; |
Conditions | Yield |
---|---|
under acetone, in presence chalk; |
gold(III) chloride
5-(3,4,5-trimethoxybenzyl)pyrimidine-2,4-diamine
Conditions | Yield |
---|---|
In methanol adding soln. of AuCl3 to soln. of trimethoprim in methanol; stirring for 24h at room temp.; evapn. (vac., 50°C), addn. of ether containing some MeOH, pptn.,filtn., dissolving in methanol, pptn. with ether, (this step was repeated three times), filtration, washing with ether, drying in vac. over P4O10 at 100°C; elem. anal.; | 64% |
N,N-dimethylthioformamide
gold(III) chloride
(gold(III) trichloride (N,N'-dimethylthioformamide))
Conditions | Yield |
---|---|
In tetrahydrofuran addn. of AuCl3 to a soln. of N,N'-dimethylthioformamide in THF (under Ar), stirring at room temp. for 4 h; filtn. through anhydrous MgSO4, reducing volume in vacuo, slow addn. of pentane, soln. is left at -30°C until crystals appeared, decanting, drying in vacuo, elem. anal.; | 62% |
2-(4-methoxybenzylidene)-N-phenylhydrazinecarbothioamide
gold(III) chloride
Conditions | Yield |
---|---|
In methanol refluxed for about 30 min,pptn.; ppt. washed with water, dried under reduced pressure for 24 h, elem. anal.; | 60% |
Primaquine
gold(III) chloride
Conditions | Yield |
---|---|
In ethanol; water 1:1 aq. ethanolic soln. of AuCl3 and the ligand (in 1:3 molar ratio) was refluxed for about 1 h; concd., cooled to room temp., ppt. was sepd., washed with ice cold aq. ethanol, dried at room temp. over P4O10 under vac., recrystd. from acetone; elem. anal.; | 60% |
Conditions | Yield |
---|---|
In neat (no solvent) vac.; equimolar ratio, chemical transport (230-215°C, several d); | 60% |
gold(III) chloride
[Ir(NH3)5Cl](2+)*[AuCl4](1-)*Cl(1-)=[Ir(NH3)5Cl][AuCl4]Cl
Conditions | Yield |
---|---|
In water addn. of freshly prepared aq. soln. of AuCl3 to warm aq. soln. of (Ir(NH3)5Cl)Cl2 (40°C) in ratio Ir-to-Au 1:1; crystn. for 2 h; filtration in vac., washing with min. amt. of H2O; drying in air; | 60% |
Conditions | Yield |
---|---|
Stage #1: gold(III) chloride; 2-mesitylmagnesium bromide In tetrahydrofuran at -80℃; for 3h; Inert atmosphere; Schlenk technique; Stage #2: In tetrahydrofuran; 1,4-dioxane at 20℃; for 0.5h; Inert atmosphere; Schlenk technique; | 55% |
gold(III) chloride
Conditions | Yield |
---|---|
With dimethyl sulfoxide In ethanol; chloroform anhydrous conditions, DMSO added to soln. of AuCl3 in chloroform with 4% ethanol; precipitate filtered, washed with ether, dried in vacuum, elem. anal.; | 53% |
Conditions | Yield |
---|---|
byproducts: SO2, SO3; in melt; |
Conditions | Yield |
---|---|
With hydrogenchloride In water heating in sealed tube, 100°C; |
gold(III) chloride
Conditions | Yield |
---|---|
With thionyl chloride In neat (no solvent) heating in sealed tube, 200°C (minimum 10 days); | |
With chlorine gaseous Cl2, at moderated temp.; | |
With chlorine gaseous Cl2, in presence of moisture, at ambient temp.; |
Conditions | Yield |
---|---|
In not given Kinetics; | |
In not given Kinetics; |
Conditions | Yield |
---|---|
In neat (no solvent) 200°C; 10 d (small yield);; | |
In neat (no solvent) 200°C; 10 d (small yield);; |
Conditions | Yield |
---|---|
under acetone, in presence chalk; |
Conditions | Yield |
---|---|
In not given |
phosphorus pentachloride
gold(III) chloride
Conditions | Yield |
---|---|
byproducts: PCl3; |
Conditions | Yield |
---|---|
In neat (no solvent) slow reaction;; | |
In neat (no solvent) passing gaseous chlorine ovver gold sponge at 265°C;; recrystd. on the cool wall of reactor;; | |
In neat (no solvent) reacted at 250°C; sublimated at 250-280°C; |
Conditions | Yield |
---|---|
In neat (no solvent) powdery Au; at 180 to 190°C;; AuCl and small amounts of AuCl3 obtained;; | |
In neat (no solvent) powdery Au; at 180 to 190°C;; AuCl and small amounts of AuCl3 obtained;; |
Conditions | Yield |
---|---|
In further solvent(s) byproducts: AgCl, K2CO3; in abs. alc.; | |
In further solvent(s) byproducts: AgCl, K2CO3; in abs. alc.; |
Conditions | Yield |
---|---|
In water | |
In water |
gold(III) chloride
Conditions | Yield |
---|---|
With SOCl2 In thionyl chloride byproducts: SO2, HCl; HAuCl4*3H2O heated under reflux with SOCl2; remaining SOCl2 removed by syringe; ppt. dried in vac. at 65°C for 4 h; |
Conditions | Yield |
---|---|
15°C; on surface of rest of Au pptd. As; AuCl3 dissolved in AsCl3; | |
15°C; on surface of rest of Au pptd. As; AuCl3 dissolved in AsCl3; |
Conditions | Yield |
---|---|
In neat (no solvent) some hours (160°C); gold powder;; |
Conditions | Yield |
---|---|
With nitric acid dissolving Au in aqua regia by mild heating (60 ° C) under N2; heating for several hours at 140 ° C;; | |
With HNO3 In hydrogenchloride; nitric acid gold was dissolved in aqua regia; heating in a mineral oil bath at 120°C for 3 h;; |
silver tetrachloroaurate(III)
gold(III) chloride
Conditions | Yield |
---|---|
byproducts: AgCl; decompn.; | |
byproducts: AgCl; decompn.; |
gold(III) chloride
Conditions | Yield |
---|---|
In thionyl chloride stirring for 3 days, color changed from yellow to orange; removing thionyl chloride; drying (vac., room temp.); |
Conditions | Yield |
---|---|
In neat (no solvent) exposing H(AuCl4)*(H2O)x in dry dichlorine flow at 200°C for 30 min (Handbuch der praeparativen unorganishen Chemie, Ed. by G. Brauer (Ferdinand Enke, Stuttgart, 1981; Mir, Moscow, 1985), vol. 3); |
gold(III) chloride
Conditions | Yield |
---|---|
With water byproducts: HCl, H3PO4; effect of moisture; | |
byproducts: phosphoric acid; evapn. in vac.; | |
byproducts: phosphoric acid; evapn. in vac.; | |
With H2O byproducts: HCl, H3PO4; effect of moisture; |
A
phosphorus pentachloride
B
gold(III) chloride
Conditions | Yield |
---|---|
120°C; reaction started at ambient temp. (PCl5 gas developed); | |
120°C; reaction started at ambient temp. (PCl5 gas developed); |
Conditions | Yield |
---|---|
With hydrogenchloride | |
With HCl |
Conditions | Yield |
---|---|
With hydrogenchloride | |
With HCl |
gold(III) chloride
Conditions | Yield |
---|---|
With tin chloride also formed a double derivative of tin chloride with SCl4; | |
With tin chloride also formed a double derivative of tin chloride with SCl4; |
Conditions | Yield |
---|---|
also formed a double derivative of AsCl3 with SCl4; | |
also formed a double derivative of AsCl3 with SCl4; |
antimonypentachloride
gold(III) chloride
Conditions | Yield |
---|---|
also formed a double derivative of SbCl5 with SCl4; | |
also formed a double derivative of SbCl5 with SCl4; |
Conditions | Yield |
---|---|
In further solvent(s) byproducts: COF2; absence of air and moisture; stirring AuCl3 in SbF5 under 0.6 atm CO (60-70°C, 5 d); evapn. (vac., 55°C); | 99% |
Conditions | Yield |
---|---|
In melt in pyridinium chloride melt; | 95% |
In water | |
In not given excess AuCl3; slow redn.; | |
In hydrogenchloride fast redn.; | |
In not given excess AuCl3; slow redn.; |
Conditions | Yield |
---|---|
In melt in pyridinium chloride melt; | 95% |
In not given | |
In further solvent(s) in melted pyridinium hydrogenchloride (C5H6NHCl2); |
Conditions | Yield |
---|---|
In melt in pyridinium chloride melt; | 95% |
In not given excess AuCl3; slow redn.; | |
In hydrogenchloride moderate redn.; | |
In not given excess AuCl3; slow redn.; |
gold(III) chloride
bis(N,N-di-iso-butyldithiocarbamato-S,S')gold(III) tetrachloroaurate(III)
Conditions | Yield |
---|---|
With HCl In hydrogenchloride; water to corresponding Cd compd. soln. of AuCl3 in 2 M HCl added dropwise, stirred for 1 h; recrystn. (acetone); XRD; | 93% |
gold(III) chloride
Conditions | Yield |
---|---|
With HCl In hydrogenchloride; water to corresponding Cd compd. soln. of AuCl3 in 2 M HCl added dropwise, stirred for 1 h; recrystn. (EtOH); XRD; | 91% |
N,N,N'-tris(trimethylsilyl)benzamidine
gold(III) chloride
N,N'-bis(trimethylsilyl)benzamidinato-dichlorogold
Conditions | Yield |
---|---|
In dichloromethane byproducts: ClSi(CH3)3; tris(trimethylsilyl)benzamidine added to a stirred suspension of AuCl3 in CH2Cl2 at 0°C, cooling removed, filtered; solvent removed, cooled down to 4°C, washed (cold CH2Cl2), dried in vacuo; elem. anal., IR; | 90% |
gold(III) chloride
Conditions | Yield |
---|---|
With HCl In hydrogenchloride; water to corresponding Cd compd. soln. of AuCl3 in 2 M HCl added dropwise, stirred for 1 h; recrystn. (MeOH); XRD; | 89% |
Conditions | Yield |
---|---|
With carbon monoxide In dichloromethane CH2Cl2 soln. of anhyd. AuCl3 was stirred under carbon monoxide at atmospheric pressure at room temp. for 12 h, treated with a CH2Cl2 soln. of norbornene, stirred for 3 h at room temp.; evapd., pentane was added, the product was filtered and dried in vac.; elem. anal.; | 88% |
gold(III) chloride
bis(N,N-di-iso-propyldithiocarbamato-S,S')gold(III) tetrachloroaurate(III)
Conditions | Yield |
---|---|
With HCl In hydrogenchloride; water to corresponding Cd compd. soln. of AuCl3 in 2 M HCl added dropwise, stirred for 1 h; recrystn. (acetone); XRD; | 87% |
Conditions | Yield |
---|---|
In thionyl chloride suspn. of anhyd. AuCl3 in SOCl2 stirred, dry CO, 1 h), red soln. filtered, CO uptake continued for 18 h (slow agitation); hexane added to soln. (CO atmosphere), crystals washed with CO-satd. hexane, dried (CO); | 82.5% |
gold(III) chloride
Au(py)Cl3
Conditions | Yield |
---|---|
With C5H5N In water AuCl3 was dissolved in H2O and pyridine was added with stirring;; the ppt. was dried under vacuum;; | 82% |
gold(III) chloride
Conditions | Yield |
---|---|
In water to aq. soln. K10(P2W20(OH2)2O70)*22H2O AuCl3 was added and stirred at 55°C for 2 h; soln. was cooled to room temp. and filtered, after 2 days at room temp. ppt. was filtered and dried under suction for 12 h; elem. anal.; | 78% |
2-(2-phenylpropan-2-yl)pyridine
gold(III) chloride
HNC5H4C(CH3)2C6H5(1+)*AuCl4(1-)=[HNC5H4C(CH3)2C6H5][AuCl4]
Conditions | Yield |
---|---|
In chloroform stirring (room temp., 1 h); concn., pptn. on Et2O addn.; | 73% |
Conditions | Yield |
---|---|
With CO In thionyl chloride AuCl3 suspended in SOCl2 under N2, reaction flask evacuated, filled with CO at atm. pressure, stirred at 20.1°C until Au2Cl6 disappeared(36 h); filtration, drying in vac.; | A n/a B 67% |
gold(III) chloride
5-(3,4,5-trimethoxybenzyl)pyrimidine-2,4-diamine
Conditions | Yield |
---|---|
In methanol adding soln. of AuCl3 to soln. of trimethoprim in methanol; stirring for 24h at room temp.; evapn. (vac., 50°C), addn. of ether containing some MeOH, pptn.,filtn., dissolving in methanol, pptn. with ether, (this step was repeated three times), filtration, washing with ether, drying in vac. over P4O10 at 100°C; elem. anal.; | 64% |
This chemical is called Gold trichloride, and it's also named as Gold chloride. With the classification codes of Mutation data; Reproductive Effect, its product categories are Inorganics; Gold Catalysts Metal and Ceramic Science; Gold Salts; Gold Catalysis and Inorganic Chemistry; GoldMetal and Ceramic Science; Catalysis and Inorganic Chemistry; Chemical Synthesis; Crystal Grade Inorganics. The CAS registry number of this chemical is 13453-07-1. Additionally, it's soluble in water.
Other characteristics of the chemical can be summarised as followings: (1)H-Bond Donor: 0; (2)H-Bond Acceptor: 0; (3)Rotatable Bond Count: 0; (4)Exact Mass: 301.87311; (5)MonoIsotopic Mass: 301.87311; (6)Topological Polar Surface Area: 0; (7)Heavy Atom Count: 4; (8)Formal Charge: 0; (9)Complexity: 8; (10)Isotope Atom Count: 0; (11)Covalently-Bonded Unit Count: 1.
When you are using this chemical, please be cautious about it as the following: This chemical is irritating to eyes, respiratory system and skin. You should wear suitable protective clothing if you use it. In case of contacting with eyes, rinse immediately with plenty of water and seek medical advice.
You can still convert the following datas into molecular structure:
1.SMILES: Cl[Au](Cl)Cl
2.InChI: InChI=1/Au.3ClH/h;3*1H/q+3;;;/p-3/rAuCl3/c2-1(3)4
3.InChIKey: RJHLTVSLYWWTEF-LZHUSIJAAG
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