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inquiryItems Standard Result Assay 98%min ----------------------------------------------------------------------------------------------
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inquiryConditions | Yield |
---|---|
{[Cu{[(1-vinylIm-2-yl)CH2]3N}Cl]PF6}-{[CH2=C(CH3)CO2CH2-]n} In water; dimethyl sulfoxide at 50℃; for 96h; pH=9.5; Kinetics; Further Variations:; Catalysts; pH-values; Temperatures; catalyst ratios; | 53% |
B
disodium (4-nitrophenyl)phosphate
Conditions | Yield |
---|---|
With sodium chloride In d(4)-methanol at 65℃; Equilibrium constant; |
sodium bis(4-nitrophenyl) phosphate
A
4-nitro-phenol
B
disodium (4-nitrophenyl)phosphate
Conditions | Yield |
---|---|
With [D]-sodium hydroxide; (Et2NH2)8[{α-PW11O39Zr(μ-OH)(H2O)}2]*7H2O; sodium diphenyl phosphate; hydrogen chloride In water-d2 at 60℃; pH=6.4; Kinetics; Reagent/catalyst; Temperature; Concentration; |
Conditions | Yield |
---|---|
Multi-step reaction with 4 steps 1: triethylamine / dichloromethane / 4 h / 20 °C 2: acetonitrile / 16 h / 0 - 20 °C 3: water / methanol / 1 h / 0 - 20 °C 4: sodium hydroxide / water / 0 °C / Cooling with ice View Scheme | |
Multi-step reaction with 4 steps 1: triethylamine / dichloromethane / 4 h / 20 °C 2: acetonitrile / 24 h / 0 - 20 °C 3: water / methanol / 1 h / 0 - 20 °C 4: sodium hydroxide / water / 0 °C / Cooling with ice View Scheme |
Conditions | Yield |
---|---|
Multi-step reaction with 3 steps 1: acetonitrile / 16 h / 0 - 20 °C 2: water / methanol / 1 h / 0 - 20 °C 3: sodium hydroxide / water / 0 °C / Cooling with ice View Scheme | |
Multi-step reaction with 3 steps 1: acetonitrile / 24 h / 0 - 20 °C 2: water / methanol / 1 h / 0 - 20 °C 3: sodium hydroxide / water / 0 °C / Cooling with ice View Scheme |
disodium (4-nitrophenyl)phosphate
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: water / methanol / 1 h / 0 - 20 °C 2: sodium hydroxide / water / 0 °C / Cooling with ice View Scheme |
Conditions | Yield |
---|---|
With sodium hydroxide In water at 0℃; Cooling with ice; | 297 g |
disodium (4-nitrophenyl)phosphate
Conditions | Yield |
---|---|
In water 1:1 mixt. of Zn complex and p-nitrophenyl phosphate disodium salt; | 99% |
bis(N,N-dimethylformamide)dichloridodioxidomolybdenum(VI)
disodium (4-nitrophenyl)phosphate
Conditions | Yield |
---|---|
With water at 55℃; for 0.5h; | 95% |
Conditions | Yield |
---|---|
With cerium(IV) oxide In ethanol at 25℃; for 8h; Kinetics; | 91% |
With tetraethylammonium hydroxide In water; acetonitrile at 20℃; | |
at 37℃; enzimatically by alkaline and acid phosphatase; |
disodium (4-nitrophenyl)phosphate
Conditions | Yield |
---|---|
With NaOH In water adding aq. soln. of amine to Zn salt, adding aq. NaOH, stirring for 1 h at 45°C, filtration, adding. aq. soln. of p-nitrophenyl phosphatedisodium salt; cooling to room temp.; elem. anal.; | 80% |
disodium (4-nitrophenyl)phosphate
Conditions | Yield |
---|---|
With HEPES buffer; NaClO4 In water soln. of Cu complex, Na2O2P(O)OC6H4NO2, HEPES buffer (pH 7.4) and NaClO4kept at 38°C overnight; crystals collected; washed with water; elem. anal.; | 70% |
disodium (4-nitrophenyl)phosphate
Conditions | Yield |
---|---|
With HClO4 In water stirring (60°C), 2 d), adjustment of pH to 3 (HClO4), evapn. of solvent; recrystn. (water); elem. anal.; | 69% |
Conditions | Yield |
---|---|
With NaOH In water aq. soln. of Zn salt added to aq. soln. of HCl salt of ligand; 0.10 M NaOH (5 equiv.) added dropwise at 45°C for 1 h; soln. filtered withcellulose nitrate filter; Na phosphate added; cooled to room temp.; elem. anal.; | 69% |
disodium (4-nitrophenyl)phosphate
A
[Co(tris(2-pyridylmethyl)amine)(phosphate)]
Conditions | Yield |
---|---|
With charcoal; NaOH In water to a soln. of Co-complex added a soln. of disodium 4-nitrophenylphosphate; mixed soln. adjusted to pH 3 with NaOH soln.; heating to 60°C and catalytic amount of active charcoal added; stirred at 60°C for 7 h; soln. neutralized and products purified by column chromy. with cation-exchange resin; | A 8% B 51% |
With charcoal; NaOH In water to a soln. of Co-complex added a soln. of disodium 4-nitrophenylphosphate; mixed soln. adjusted to pH 3 with NaOH soln.; heating to 60°C and catalytic amount of active charcoal added; stirred at 60°C for 5 h; soln. neutralized and products purified by column chromy. with cation-exchange resin; | A n/a B 46% |
With charcoal; NaOH In water to a soln. of Co-complex added a soln. of disodium 4-nitrophenylphosphate; mixed soln. adjusted to pH 3 with NaOH soln.; heating to 60°C and catalytic amount of active charcoal added; stirred at 60°C for 3 h; soln. neutralized and products purified by column chromy. with cation-exchange resin; | A n/a B 26% |
Conditions | Yield |
---|---|
In methanol; dichloromethane soln. disodium 4-nitrophenylphosphate in MeOH-CH2Cl2 was added to soln. Cu complex in MeOH and stirred at room temp. for 12 h; solvent was evapd. in vacuo, residue was extd. with MeOH and concd., Et2O was added; elem. anal.; | 28% |
disodium (4-nitrophenyl)phosphate
methyloxirane
Conditions | Yield |
---|---|
Stage #1: disodium (4-nitrophenyl)phosphate; methyloxirane With ammonium hydroxide In water at 35℃; Stage #2: With barium dihydroxide at 20℃; pH=Ca.7; | 0.4% |
tetraethylammonium hydroxide
disodium (4-nitrophenyl)phosphate
Tentraethylammonium 4-nitrophenoxide
Conditions | Yield |
---|---|
With water In acetonitrile at 20℃; Rate constant; Mechanism; Thermodynamic data; ΔH(excit.), ΔS(excit.); other concentration of water , Et4N(1+)*OH(1-) and temperatures; |
disodium (4-nitrophenyl)phosphate
p-nitrophenolate
Conditions | Yield |
---|---|
With water; Zn*(im-bzl-L-His)2dien at 35 - 50℃; Kinetics; | |
With C91H151N3O70Zn In water at 35℃; pH=6.5 - 9.5; Kinetics; pH-value; Good's buffer; | |
With [Zn2(2-[bis(2-methoxyethyl)aminomethyl]-4-methylphenol)2Cl2] In water; N,N-dimethyl-formamide Kinetics; Reagent/catalyst; Concentration; |
Conditions | Yield |
---|---|
With pentan-1-ol; sodium citrate; erythrocyte acid phosphatase (EAPase) at 37℃; for 0.166667h; Mechanism; pH=5.5, effects of various alcohols on EAPase and Prostatic acid phosphatase (PAPase) enzymes activity, Km, Vmax constants; |
disodium (4-nitrophenyl)phosphate
Conditions | Yield |
---|---|
With NaOH In water byproducts: (NH2C2H4)3NCo(O2P(O)O)CoN(C2H4NH2)3(3+), (NH2C2H4)3NCo(OH)(OPO3)]; 40°C, pH from 4.61 to 8.44; not sepd., detected by NMR spectra; |
trans-dichlorobis(ethylenediamine)cobalt(III) chloride
disodium (4-nitrophenyl)phosphate
cis-p-nitrophenylphosphatobis(ethylenediamine)cobalt(III) chloride
Conditions | Yield |
---|---|
In water mixing into a past using a few drops of water; warming for a few min atca 60°C; diln. with water; heating for 5-10 min at 60-70°C; filtration, washing with water, EtOH, Et2O; drying in vac.; elem. anal.; |
disodium (4-nitrophenyl)phosphate
Conditions | Yield |
---|---|
With NaOH In water 25°C, pH from 4.88 to 8.01; not sepd., detected by NMR spectra; |
disodium (4-nitrophenyl)phosphate
Conditions | Yield |
---|---|
In water Kinetics; 15°C, pH 4.57; not sepd., detected by NMR spectra; |
disodium (4-nitrophenyl)phosphate
Conditions | Yield |
---|---|
With triethanolamine; riboflavin In water at 40℃; for 4h; UV-irradiation; | |
With hydrogen; palladium 10% on activated carbon In ethanol; water at 20℃; under 1551.49 Torr; for 2h; |
sodium methylate
disodium (4-nitrophenyl)phosphate
bis-sodium salt of methyl phosphate
Conditions | Yield |
---|---|
In methanol; d(4)-methanol at 50℃; Kinetics; Reagent/catalyst; pH-value; Time; |
disodium (4-nitrophenyl)phosphate
Conditions | Yield |
---|---|
In d(4)-methanol at 65℃; Equilibrium constant; |
disodium (4-nitrophenyl)phosphate
Conditions | Yield |
---|---|
In water; dimethyl sulfoxide at 25℃; |
disodium (4-nitrophenyl)phosphate
Conditions | Yield |
---|---|
In water; dimethyl sulfoxide at 25℃; |
disodium (4-nitrophenyl)phosphate
Conditions | Yield |
---|---|
In water; dimethyl sulfoxide at 25℃; |
disodium (4-nitrophenyl)phosphate
alanine isopropyl ester hydrochloride
triethylamine
Conditions | Yield |
---|---|
With dicyclohexyl-carbodiimide In water; tert-butyl alcohol Reflux; |
disodium (4-nitrophenyl)phosphate
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: dicyclohexyl-carbodiimide / tert-butyl alcohol; water / Reflux 2: N,N-dimethyl-formamide / 1 h / 25 °C / Inert atmosphere View Scheme |
disodium (4-nitrophenyl)phosphate
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: hydrogen / palladium 10% on activated carbon / ethanol; water / 2 h / 20 °C / 1551.49 Torr 2: N,N-dimethyl-formamide / 3 h / 90 °C View Scheme |
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