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inquiryProduct Name 5-Nitro-1,10-phenathroline Structural formula CAS No. 4199-88-6 Appearance:Pale yellow or brown solid Melting point:198-200°C Content:≥98.0% Appearance:brown powder Storage:Stor
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inquiryProduct Name: 5-Nitro-1,10-phenanthroline CAS: 4199-88-6 MF: C12H7N3O2 MW: 225.2 EINECS: 224-097-6 Product Categories: Mol File: 4199-88-6.mol 5-Nitro-1,10-phenanthroline Structure 5-Nitro-1,10-phenanthroline Chemical Properti
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Conditions | Yield |
---|---|
With sulfuric acid; nitric acid at 160℃; for 3h; | 100% |
With sulfuric acid; nitric acid at 160℃; | 99% |
With sulfuric acid; nitric acid at 160℃; for 3h; | 99% |
1,10-phenanthroline-5-carboxylic acid
5-Nitro-1,10-phenanthroline
Conditions | Yield |
---|---|
With nitronium tetrafluoborate; silver carbonate In N,N-dimethyl acetamide at 90℃; for 12h; Inert atmosphere; Schlenk technique; regioselective reaction; | 81% |
1,10-Phenanthroline
A
1,10-phenanthroline-5,6-dione
B
5-Nitro-1,10-phenanthroline
Conditions | Yield |
---|---|
With sulfuric acid; nitric acid for 1.5h; Heating; | A 20% B 18.7 g |
Conditions | Yield |
---|---|
With sulfuric acid; orthoarsenic acid |
1,10-Phenanthroline
sulfuric acid
sulfur trioxide
nitric acid
A
4,5-Diazafluoren-9-one
B
5-Nitro-1,10-phenanthroline
Conditions | Yield |
---|---|
at 170℃; |
1,10-Phenanthroline
sulfuric acid
sulfur trioxide
nitric acid
A
1,10-phenanthroline-5,6-dione
B
5-Nitro-1,10-phenanthroline
Conditions | Yield |
---|---|
at 170℃; |
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: glycerol; H3aso4; aqueous H2SO4 2: H2SO4; concentrated HNO3 View Scheme |
Conditions | Yield |
---|---|
With sulfuric acid; nitric acid | 1.49 g (42%) |
5-Nitro-1,10-phenanthroline
1,10-phenanthroline-5-amine
Conditions | Yield |
---|---|
With hydrogen; palladium on activated charcoal In methanol under 2280.15 Torr; for 1h; | 100% |
With 10% Pd/C; hydrogen In methanol under 2280.15 Torr; for 1h; | 100% |
With hydrazine hydrate; palladium 10% on activated carbon In ethanol for 4h; Reflux; | 98% |
ammonium pertechnetate
5-Nitro-1,10-phenanthroline
Conditions | Yield |
---|---|
With hydrogenchloride In methanol 5-nitro-1,10-phenanthroline dissolved in MeOH by gentle heating, cooled to ambient temp., addn. of Tc-compd. with stirring, dropwise addn. of concd. HCl; cooled to -20°C, ppt. collected, washed with MeOH, dried in vac. overnight; elem. anal.; | 99% |
dichloro(benzene)ruthenium(II) dimer
dichloromethane
5-Nitro-1,10-phenanthroline
Conditions | Yield |
---|---|
In dichloromethane inert atm.; 2 equiv of phenanthroline was added to a suspn. of complex in CH2Cl2, the mixt. was stirred for 3 h at room temp.; evapd. to dryness, dissolved in water, filtered, evapd. to dryness; elem. anal.; | 99% |
5-Nitro-1,10-phenanthroline
[(η6-hexamethylbenzene)Ru(η2-5-nitro-1,10-phenanthroline)Cl]Cl
Conditions | Yield |
---|---|
In dichloromethane inert atm.; 2 equiv of phenanthroline was added to a suspn. of complex in CH2Cl2, the mixt. was stirred for 3 h at room temp.; evapd. to dryness, dissolved in water, filtered, evapd. to dryness; elem. anal.; | 99% |
[ruthenium(II)(η6-1-methyl-4-isopropyl-benzene)(chloride)(μ-chloride)]2
5-Nitro-1,10-phenanthroline
[(η6-p-cymene)Ru(nitrophen)Cl]Cl
Conditions | Yield |
---|---|
In dichloromethane inert atm.; 2 equiv of phenanthroline was added to a suspn. of complex in CH2Cl2, the mixt. was stirred for 3 h at room temp.; evapd. to dryness, dissolved in water, filtered, evapd. to dryness; elem. anal.; | 99% |
In dichloromethane for 2h; Reflux; |
5-Nitro-1,10-phenanthroline
N-benzyl-N-(methoxymethyl)-N-[(trimethylsilyl)methyl]amine
Conditions | Yield |
---|---|
With trifluoroacetic acid In dichloromethane at 0 - 20℃; for 5h; Inert atmosphere; | 99% |
5-Nitro-1,10-phenanthroline
(Pd(5-nitro-1,10-phenanthroline)(SCN)2)
Conditions | Yield |
---|---|
In ethanol dropwise addn. of stoich. amt. of ligand to Pd-complex (60°C, pptn.); filtration, washing (H2O, EtOH, Et2O), drying (in air); elem. anal.; | 96% |
5-Nitro-1,10-phenanthroline
Conditions | Yield |
---|---|
Stage #1: 5-Nitro-1,10-phenanthroline; C116H84Cl2Ir2N8 In methanol; dichloromethane for 6h; Reflux; Stage #2: ammonium hexafluorophosphate In methanol; dichloromethane for 0.25h; | 95% |
5-Nitro-1,10-phenanthroline
[{(η3-C3H4COOMe)Mo(CO)2(NCMe)(μ-Br)}2]
[(η3-C3H4COOMe)Mo(CO)2(5-NO2-phen)Br]
Conditions | Yield |
---|---|
In dichloromethane at 20℃; for 0.5h; Inert atmosphere; | 94% |
Conditions | Yield |
---|---|
In acetonitrile dissolving of Cu(BF4)2 hydrate (1 equiv.) in CH3CN, addn. dropwise of soln. of NO2C12H7N2 (2 equiv.) in CH3CN; removal of solvent by rotary evapn.; | 93.01% |
5-Nitro-1,10-phenanthroline
[(η3-C3H5)Mo(CO)2(5-NO2-phen)Cl]
Conditions | Yield |
---|---|
In dichloromethane at 20℃; for 0.5h; Inert atmosphere; | 93% |
5-Nitro-1,10-phenanthroline
Conditions | Yield |
---|---|
With piperidinium 2-chloroterephthalate In methanol addn. of soln. of nitrophenanthroline to soln. of Mn salt and piperidinium chloroterephthalate, stirring (6 h, room temp.; pptn.); filtration, washing (EtOH, Et2O), drying (vac.); elem. anal.; | 92% |
5-Nitro-1,10-phenanthroline
Conditions | Yield |
---|---|
In dichloromethane for 2h; Inert atmosphere; | 92% |
N,N'-bis<2-(dimethylamino)ethyl>oxamide
5-Nitro-1,10-phenanthroline
Conditions | Yield |
---|---|
With triethylamine In methanol to soln. of oxamide stirred in MeOH added soln. of Cu(ClO4)2*6H2O in MeOH and Et3N; soln. stirred for 30 min at room temp.; filtered; to filtrate added soln. of Mn(ClO4)2*6H2O in MeOH and 5-NO2-1,10-phenanthroline inMeOH under N2; mixt. stirred for 5 h; crystals filtered; washed (MeOH, H2O, Et2O); dried (P2O5, vac.); recrystd. (DMF/EtOH (1:1)); elem. anal.; | 90% |
N,N'-bis(3-aminopropyl)oxamido copper(II)
5-Nitro-1,10-phenanthroline
Conditions | Yield |
---|---|
With ethyl orthoformate In ethanol elem. anal.; | 90% |
5-Nitro-1,10-phenanthroline
Conditions | Yield |
---|---|
In water suspn. of bis(2,2'-bipyridine)RuCl2 and 5-nitro-1,10-phenanthroline in water refluxed for 1 h; resulting soln. cooled and filtrated; filtrate evapd. under vac. and residue dissolved in methanol and repptd. into abs. diethyl ether; chromy., NMR; | 90% |
Conditions | Yield |
---|---|
In toluene for 2h; Reflux; | 90% |
5-Nitro-1,10-phenanthroline
Conditions | Yield |
---|---|
Stage #1: 5-Nitro-1,10-phenanthroline; C116H84Cl2Ir2N8 In methanol; dichloromethane for 6h; Reflux; Stage #2: ammonium hexafluorophosphate In methanol; dichloromethane for 0.25h; | 90% |
5-Nitro-1,10-phenanthroline
N,N'-bis(3-dimethylaminopropyl)oxalamide
Conditions | Yield |
---|---|
With triethylamine In methanol; ethanol addn. of soln. of Cu(NO3)2*3H2O and Et3N (2 equiv.) in MeOH to stirred soln. of (Me2NC3H6NHCO)2 in MeOH; stirring at room temp. for 30 min; filtration, addn. of soln. of Gd(NO3)3*6H2O and 5-NO2-phen (2 equiv.) in EtOH to filtrate, pptn., reflux for 9 h; crystn., filtration, washing several times with MeOH, water and Et2O, drying over P2O5 under reduced pressure, recrystn. from DMF/EtOH (1:3); elem. anal.; | 89% |
5-Nitro-1,10-phenanthroline
Conditions | Yield |
---|---|
Stage #1: 5-Nitro-1,10-phenanthroline; C116H84Cl2Ir2N8 In methanol; dichloromethane for 6h; Reflux; Stage #2: ammonium hexafluorophosphate In methanol; dichloromethane for 0.25h; | 89% |
5-Nitro-1,10-phenanthroline
Conditions | Yield |
---|---|
With ethyl orthoformate In ethanol; acetonitrile addn. of a soln. of chromium salt in abs. EtOH to a stirred soln. of piperidinium terephthalate in CH3CN, addn. of ethyl orthoformate, addn. ofa soln. of bpy in abs. EtOH, refluxing for 2 h; filtration, washing with EtOH and Et2O several times, drying over P2O5 in vac., recrystn (DMF); elem. anal.; | 88% |
5-Nitro-1,10-phenanthroline
Conditions | Yield |
---|---|
With piperidinium 4-nitrophthalate salt In methanol stirring (room temp., 6 h); ppt. washing (methanol, Et2O), drying (vac.); elem. anal.; | 88% |
Conditions | Yield |
---|---|
Stage #1: copper(II) nitrate trihydrate; 4,4,4-trifluoro-1-(2-furanyl)-1,3-butanedione In methanol at 20℃; for 4h; Stage #2: 5-Nitro-1,10-phenanthroline In methanol at 20℃; for 24h; | 88% |
Ethyl isocyanoacetate
5-Nitro-1,10-phenanthroline
Ethyl 2H-dibenzoisoindole-1-carboxylate
Conditions | Yield |
---|---|
With 1,8-diazabicyclo[5.4.0]undec-7-ene In tetrahydrofuran for 4h; Ambient temperature; | 87% |
With 1,8-diazabicyclo[5.4.0]undec-7-ene In tetrahydrofuran at 20℃; | 76% |
With 1,8-diazabicyclo[5.4.0]undec-7-ene In tetrahydrofuran Ambient temperature; | 53% |
5-Nitro-1,10-phenanthroline
ethyl 2-cyanoacetate
Ethyl 2H-dibenzoisoindole-1-carboxylate
Conditions | Yield |
---|---|
With 1,8-diazabicyclo[5.4.0]undec-7-ene In tetrahydrofuran for 8h; Ambient temperature; | 87% |
5-Nitro-1,10-phenanthroline
C56H31ClN12O12Fe2(2+)*SO4(2-)
Conditions | Yield |
---|---|
In methanol mixt. in MeOH was stirred at room temp. for 6 h under N2; filtered, washed with MeOH and Et2O, dried over P2O5 under reduced pressure, recrystd. from DMF-EtOH; elem. anal.; | 87% |
Conditions | Yield |
---|---|
In ethanol; acetonitrile dropwise addn. of soln. of Ln(ClO4)2 (in EtOH) and sol. of nitrophenanthroline (in MeCN) to soln. of isophthalate (in EtOH) (stirring), refluxing (18 h; pptn.); filtration, washing (EtOH, MeCN, Me2O), drying (over P2O5, vac.), recrystn. (DMF/EtOH 2 : 1); elem. anal.; | A 87% B n/a |
5-Nitro-1,10-phenanthroline
[Ir(2-phenylpyridine(-H))2(5-nitro-1,10-phenanthroline)](hexafluorophosphate)
Conditions | Yield |
---|---|
In methanol; dichloromethane (N2); refluxing soln. of iridium compd. and phenanthroline deriv. in 2:1mixt. of CH2Cl2 and methanol for 5-6 h, cooling to room temp., addn. of hexafluorophosphate salt, stirring for 15 min; filtration, evapn., dissolving in CH2Cl2, filtration, layering with ether, cooling to 0°C for overnight, isolation of crystals, elem. anal.; | 87% |
5-Nitro-1,10-phenanthroline
(S,S)-1,2-diaminocyclohexane
Conditions | Yield |
---|---|
In ethanol; water at 60℃; for 3.5h; | 87% |
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