Conditions | Yield |
---|---|
With NaOH In water; acetonitrile to aq. soln. of acid aq. soln. of NaOH added with stirring, then soln. of AgNO3 in CH3CN added under stirring; soln. slowly evapd. in air for 48 h, ppt. filtered, washed (H2O), dried (avc.); elem. anal.; | 95% |
With NaOH; acetic acid In water dissolving NaOH in water, addn. of acetic acid (several drops) and benzoic acid, addn. of resulting soln. to a satd. aq. soln. of AgNO3 in the dark; filtration, washing the residue, drying in vac.; | 80% |
With acetic acid; sodium hydroxide In water | 59% |
Conditions | Yield |
---|---|
In water dropwise addn. of a satd. aq. soln. of AgNO3 to an aq. soln. of ammonium benzoate; pptn., cooling in ice, filtration, washing (cold water, cold ethanol, ether), drying by suction; | 90% |
Conditions | Yield |
---|---|
In acetonitrile at 20℃; for 24h; Darkness; | 79% |
A
1-benzyl-2-phenyl-ethyl isocyanate
B
silver benzoate
Conditions | Yield |
---|---|
at 143℃; |
Conditions | Yield |
---|---|
In water pH 6-7; |
Conditions | Yield |
---|---|
With silver nitrate; sodium hydroxide In water |
PdITol(2,2'-bipyridine)
silver benzoate
Pd(O2CPh)Tol(2,2'-bipyridine)
Conditions | Yield |
---|---|
In dichloromethane silver aroate was added to suspn. PdITol(bpy) in CH2Cl2 and stirred for 15 min in the absence of light; soln. was filtered, filtrate was evapd. to dryness in vacuo, residue wasrinsed with n-pentane and dried in vacuo; | 100% |
silver benzoate
Conditions | Yield |
---|---|
In dichloromethane byproducts: silver bromide; under N2; react. of Ti-Cu complex with equimolar amt. of silver carboxylate in CH2Cl2 at 25°C; | 99% |
silver benzoate
Pd(O2CPh)Me(N,N,N',N'-tetramethylethylenediamine)
Conditions | Yield |
---|---|
In dichloromethane silver aroate was added to suspn. PdIMe(tmeda) in CH2Cl2 and stirred for15 min in the absence of light; soln. was filtered, filtrate was evapd. to dryness in vacuo, residue wasrinsed with n-pentane and dried in vacuo; | 99% |
silver benzoate
Pd(O2CPh)Tol(N,N,N',N'-tetramethylethylenediamine)
Conditions | Yield |
---|---|
In dichloromethane silver aroate was added to suspn. PdITol(tmeda) in CH2Cl2 and stirred for 15 min in the absence of light; soln. was filtered, filtrate was evapd. to dryness in vacuo, residue wasrinsed with n-pentane and dried in vacuo; | 99% |
[Au2Cl2(μ-2-C6F4PPh2)2]
silver benzoate
[Au2(benzoato)2(μ-2-C6F4PPh2)2]
Conditions | Yield |
---|---|
In dichloromethane a soln. of Au complex treated with Ag salt, stirred for 3 h at room temp. and shielded from light; filtered, concd. (vac.), pptd. (hexane), filtered, washed (hexane), dried; | 99% |
chloro(2,6-bis(dimethylaminomethyl)phenyl-N,C,N)palladium(II)
silver benzoate
benzoato(2,6-bis(dimethylaminomethyl)phenyl-N,C,N)palladium(II)
Conditions | Yield |
---|---|
In acetone under Ar; soln. of Pd complex in acetone added to Ag salt (molar ratio 1:1.1); stirred for 1 h in absence of light; filtered through Celite; filtrate concd. in vac.; pentane added; solid isolated; washed with pentane; dried in vac.; elem. anal.; | 98% |
silver benzoate
3,4-dihydro-dibenzacridine
trans-1,2-bis(benzoyloxy)-1,2,3,4-tetrahydrodibenzacridine
Conditions | Yield |
---|---|
In benzene for 0.333333h; Heating; | 97% |
silver benzoate
Pd(O2CPh)Me(2,2'-bipyridine)
Conditions | Yield |
---|---|
In dichloromethane silver aroate was added to suspn. PdIMe(bpy) in CH2Cl2 and stirred for 15 min in the absence of light; soln. was filtered, filtrate was evapd. to dryness in vacuo, residue wasrinsed with n-pentane and dried in vacuo; elem. anal.; | 97% |
1,2-bis[tris(trimethylsilyl)methyl]-1,2-diiododigallane
silver benzoate
bis(tris(trimethylsilyl)methyl)bis(μ-benzoate-O,O')digallium(II) diiodide
Conditions | Yield |
---|---|
In toluene byproducts: AgI; Ar, a soln. of Ga compd. added to a soln. of Ag compd. at -90°C, stirred, slowly warmed to -65°C; ppt. filtered (-70°C), solvent removed (vac., room temp.), recrystd. (cyclopentane) (from 20 to -15°C); | 97% |
Conditions | Yield |
---|---|
In dichloromethane at -40.16℃; for 3h; | 97% |
N,N,N',N'-tetramethylethylenediamine palladium(II) chloride
silver benzoate
Pd(O2CPh)2(N,N,N',N'-tetramethylethylenediamine)
Conditions | Yield |
---|---|
In dichloromethane silver aroate was added to suspn. PdCl2(tmeda) in CH2Cl2 and stirred for15 min in the absence of light; soln. was filtered, filtrate was evapd. to dryness in vacuo, residue wasrinsed with n-pentane and dried in vacuo; elem. anal.; | 96% |
bis(η5-trimethylsilylcyclopentadienyl)bis(trimethylsilylethynyl)-titanium
silver benzoate
Conditions | Yield |
---|---|
In tetrahydrofuran N2-atmosphere; stirring soln. of equimolar amts. of Ti-complex with Ag-compound at 25°C for 3 h; filtration (Celite), evapn., washing (pentane), crystn. (THF, -30°C); elem. anal.; | 95% |
chloro(2,6-bis(dimethylaminomethyl)phenyl-N,C,N)platinum(II)
silver benzoate
benzoato(2,6-bis(dimethylaminomethyl)phenyl-N,C,N)platinum(II)
Conditions | Yield |
---|---|
In acetone under Ar; soln. of Pt complex in acetone added to Ag salt (molar ratio 1:1); stirred overnight in absence of light; filtered through Celite; filtrate concd. in vac.; pentane added; solid isolated; washed with pentane; dried in vac.; elem. anal.; | 95% |
silver benzoate
Acetic acid (2S,3S,4S)-4-iodo-2-(4-methoxy-benzyl)-1-(9-phenyl-9H-fluoren-9-yl)-pyrrolidin-3-yl ester
Conditions | Yield |
---|---|
In toluene for 5h; Prevost reaction; Heating; | 94% |
dichloro(1,5-cyclooctadiene)platinum(ll)
silver benzoate
1,2-bis-(diphenylphosphino)ethane
{Pt(OCOC6H5)2(P(C6H5)2CH2CH2P(C6H5)2)}
Conditions | Yield |
---|---|
In dichloromethane addn. of dppe to a soln. of (PtCl2(cod)) in CH2Cl2, stirring (0.5 h), addn. of AgOCOPh, stirring in the absence of light (72 h); filtration, concg. the pale yellow soln., addn. of hexane, pptn., washing (hexane), drying by suction; elem. anal.; | 94% |
Conditions | Yield |
---|---|
In water High Pressure; under hydrothermal conditions; Ag(C6H5CO2), ligand and H2O sealed in Pyrex glass tube; heated at 180°C (glycerine bath) for 8 h; cooled to room temp. over 40 h; crystals sepd.; elem. anal.; | 94% |
benzyl (S)-(4-diazo-3-oxobutan-2-yl)carbamate
silver benzoate
(S)-3-benzyloxycarbonylaminobutyric acid
Conditions | Yield |
---|---|
In 1,4-dioxane; water for 6h; Reflux; | 93% |
Conditions | Yield |
---|---|
In tetrahydrofuran at 20℃; for 12h; | 93% |
In tetrahydrofuran at 20℃; for 12h; | 93% |
Conditions | Yield |
---|---|
In tetrahydrofuran at 20℃; for 12h; | 93% |
(2R,3R,4R)-N-(9-phenylfluoren-9-yl)-3-acetoxy-4-iodo-2-(p-methoxybenzyl)pyrrolidine
silver benzoate
(2R,3R,4R)-N-(9-phenylfluoren-9-yl)-4-O-benzoylanisomycin
Conditions | Yield |
---|---|
In toluene for 12h; Heating; | 92% |
(S)-3-[(benzyloxycarbonyl)amino]-1-diazo-4-phenyl-2-butanone
silver benzoate
(S)-3-benzyloxycarbonylamino-4-phenylbutyric acid
Conditions | Yield |
---|---|
In 1,4-dioxane; water for 6h; Reflux; | 92% |
silver benzoate
(S)-3-(benzyloxycarbonylamino)-4-[4-(benzyloxy)phenyl]butanoic acid
Conditions | Yield |
---|---|
In 1,4-dioxane; water for 6h; Reflux; | 92% |
Conditions | Yield |
---|---|
In tetrahydrofuran at 20℃; for 6h; Inert atmosphere; Schlenk technique; Darkness; | 92% |
Conditions | Yield |
---|---|
In tetrahydrofuran at 20℃; for 18h; | 92% |
silver benzoate
Conditions | Yield |
---|---|
In dichloromethane byproducts: AgCl, C6H5COOH; silver benzoate was added to a soln. of (C5Me5)IrCl2(Me2SO) in CH2Cl2 and stirred for 2 h at 20°C; the pptd. AgCl was filtered off, filtrate washed with sodium bicarbonatesoln. (to remove benzoic acid) and dried over sodium sulphate, solvent removed, crystd. from CH2Cl2; elem. anal.; | 91% |
In not given | 60% |
silver benzoate
Conditions | Yield |
---|---|
In tetrahydrofuran byproducts: AgCl; N2-atmosphere; equimolar amts., stirring in dark overnight; filtration (Celite), solvent removal (reduced pressure), dissoln. in CH2Cl2, filtration, crystn.; elem. anal.; | 91% |
silver benzoate
cis-[Pt(OCOPh)(κ2-C6H3-5-Me-2-PPh2)(PPh2-4-tol)]
Conditions | Yield |
---|---|
In chloroform silver benzoate was added to soln. Pt complex in CHCl3 and stirred in the dark for 15 min; ppt. was removed by centrifugation, supernatant was concd. in vacuo, n-pentane was added, ppt. was redissolved in CH2Cl2 and repptd. with n-pentane, washed with n-pentane and dried in vacuo; | A 91% B n/a |
silver benzoate
Conditions | Yield |
---|---|
With iodine In benzene for 18h; Prevost reaction; Heating; | 90.5% |
N'--N-2,4-dinitrophenyl-N-methylhydrazine
silver benzoate
O-benzoyl-NN-dimethyl-N'-(N-methyl-2,4-dinitroanilino)isourea
Conditions | Yield |
---|---|
In chloroform for 0.2h; Heating; | 90% |
The Silver benzoate, with the CAS registry number 532-31-0, is also known as Silver-benzoic acid (1:1). This chemical's molecular formula is C7H6AgO2 and molecular weight is 229.9895. What's more, its IUPAC name is called Benzoic acid; silver.
Physical properties about Silver benzoate are: (1)ACD/LogP: 1.90; (2)#of Rule of 5 Violations: 0; (3)ACD/LogD (pH 5.5): 0.58; (4)ACD/LogD (pH 7.4): -0.98; (5)ACD/BCF (pH 5.5): 1; (6)ACD/BCF (pH 7.4): 1; (7)ACD/KOC (pH 5.5): 12.43; (8)ACD/KOC (pH 7.4): 1; (9)#H bond acceptors: 2; (10)#H bond donors: 1; (11)#Freely Rotating Bonds: 1; (12)Polar Surface Area: 26.3Å2; (13)Flash Point: 111.4 °C; (14)Enthalpy of Vaporization: 51.4 kJ/mol; (15)Boiling Point: 249.3 °C at 760 mmHg; (16)Vapour Pressure: 0.0122 mmHg at 25 °C.
You can still convert the following datas into molecular structure:
(1) SMILES: [Ag].O=C(O)c1ccccc1
(2) InChI: InChI=1/C7H6O2.Ag/c8-7(9)6-4-2-1-3-5-6;/h1-5H,(H,8,9);
(3) InChIKey: GQCYXEOBZQXHPO-UHFFFAOYAJ
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