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[ CAS No. 14172-91-9 ] {[proInfo.proName]}

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Chemical Structure| 14172-91-9
Chemical Structure| 14172-91-9
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Product Details of [ 14172-91-9 ]

CAS No. :14172-91-9 MDL No. :MFCD00148862
Formula : C44H28CuN4 Boiling Point : -
Linear Structure Formula :- InChI Key :-
M.W : 676.27 Pubchem ID :-
Synonyms :

Safety of [ 14172-91-9 ]

Signal Word:Warning Class:N/A
Precautionary Statements:P261-P305+P351+P338 UN#:N/A
Hazard Statements:H302-H315-H319-H335 Packing Group:N/A
GHS Pictogram:

Application In Synthesis of [ 14172-91-9 ]

* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.

  • Downstream synthetic route of [ 14172-91-9 ]

[ 14172-91-9 ] Synthesis Path-Downstream   1~88

  • 2
  • [ 917-23-7 ]
  • copper(II) choride dihydrate [ No CAS ]
  • [ 14172-91-9 ]
  • 3
  • [ 917-23-7 ]
  • copper dichloride [ No CAS ]
  • [ 14172-91-9 ]
YieldReaction ConditionsOperation in experiment
With sodium carbonate; In water; at 350.0℃; for 0.0666667h;Inert atmosphere; Sealed tube; Using a 50 mL volumetric flask, 1.208 g of copper sulfate as a metal salt was dissolved in 50 mL of distilled water to prepare a 0.1 mol / L CuSO 4 aqueous solution. Next, 0.02 g (3.3 × 10 -5 mol) of tetraphenylporphyrin (TPP) as a compound having a porphyrin-type skeleton, 0.02 g (3.3 × 10 -5 mol) of copper sulfate Aqueous solution of sodium carbonate and 0.032 g of sodium carbonate equivalent to copper sulfate to prevent corrosion of the reaction vessel, and the interior of the reaction vessel was purged with argon and sealed. Next, the reaction vessel was charged into the sand bath set at 350 C. The reaction temperature in the reaction vessel reached the reaction temperature in about 4 minutes.
  • 4
  • [ 917-23-7 ]
  • [ 142-71-2 ]
  • [ 14172-91-9 ]
YieldReaction ConditionsOperation in experiment
400 mg With acetic acid; In chloroform; for 2h;Reflux; Copper tetraphenyl porphyrin was synthesised by taking tetra phenyl porphyrin[H2(TPP)]16(500mg) in chloroform(100ml).Copper(II) acetate(200mg) in glacial aceticacid(50ml) was added to the above solution andthe mixture was refluxed for 2hrs. The contents wereconcentrated to a volume of about 50-60ml andcooled to room temperature which resulted in crudecopper-tetraphenyl porphyrin Cu(TPP) (about450mg). The crude product was purified by columnchromatography using neutral alumina andchloroform as eluent. On elution the unreactedtetraphenyl porphyrin was eluted out first, followedby pure Cu(TPP). The chloroform fraction containingCu(TPP) was concentrated to obtain pure crystalsof Cu(TPP)[2]. The formation of Cu(TPP) wasmonitored by UV-visible spectroscopy which givepeaks-around 580, 541 and 417nm respectivelyconfirming the formation of Cu(TPP) (yield=400mg).
  • 5
  • 7,8-dihydro-5,10,15,20-tetraphenylporphyrin [ No CAS ]
  • [ 142-71-2 ]
  • [ 14172-91-9 ]
  • 7
  • [ 917-23-7 ]
  • [ 13014-03-4 ]
  • [ 14172-91-9 ]
  • 8
  • [ 917-23-7 ]
  • [ 45227-32-5 ]
  • [ 14172-91-9 ]
  • 9
  • [ 917-23-7 ]
  • [ 7787-70-4 ]
  • [ 14172-91-9 ]
  • 12
  • [ 917-23-7 ]
  • [ 377741-30-5 ]
  • [ 14172-91-9 ]
  • 13
  • [ 917-23-7 ]
  • [ 503276-25-3 ]
  • [ 14172-91-9 ]
  • 14
  • [ 917-23-7 ]
  • copper(II) nitrate [ No CAS ]
  • [ 14172-91-9 ]
YieldReaction ConditionsOperation in experiment
With sodium carbonate; In water; at 350.0℃; for 0.0666667h;Inert atmosphere; Sealed tube; Using a 50 mL volumetric flask, 1.208 g of copper sulfate as a metal salt was dissolved in 50 mL of distilled water to prepare a 0.1 mol / L CuSO 4 aqueous solution. Next, 0.02 g (3.3 × 10 -5 mol) of tetraphenylporphyrin (TPP) as a compound having a porphyrin-type skeleton, 0.02 g (3.3 × 10 -5 mol) of copper sulfate Aqueous solution of sodium carbonate and 0.032 g of sodium carbonate equivalent to copper sulfate to prevent corrosion of the reaction vessel, and the interior of the reaction vessel was purged with argon and sealed. Next, the reaction vessel was charged into the sand bath set at 350 C. The reaction temperature in the reaction vessel reached the reaction temperature in about 4 minutes.
  • 15
  • [ 917-23-7 ]
  • [ 6046-93-1 ]
  • [ 14172-91-9 ]
  • 17
  • [ 917-23-7 ]
  • copper(II) ethylenediaminetetraacetate [ No CAS ]
  • [ 14172-91-9 ]
  • 20
  • [ 917-23-7 ]
  • [ 31106-16-8 ]
  • [ 14172-91-9 ]
  • 21
  • [ 917-23-7 ]
  • [ 12320-32-0 ]
  • [ 14172-91-9 ]
  • 22
  • [ 917-23-7 ]
  • copper(II) α-nitroso-β-naphtholate [ No CAS ]
  • [ 14172-91-9 ]
  • 23
  • [ 917-23-7 ]
  • [ 34946-82-2 ]
  • [ 14172-91-9 ]
  • Cu((C6H5)4C20H10N4)(2+) [ No CAS ]
  • 25
  • copper(ll) sulfate pentahydrate [ No CAS ]
  • [ 917-23-7 ]
  • [ 14172-91-9 ]
  • 26
  • [ 917-23-7 ]
  • [ 7758-99-8 ]
  • [ 14172-91-9 ]
YieldReaction ConditionsOperation in experiment
With sodium carbonate; In water; at 350.0℃; for 0.0666667h;Inert atmosphere; Sealed tube; Using a 50 mL volumetric flask, 1.208 g of copper sulfate as a metal salt was dissolved in 50 mL of distilled water to prepare a 0.1 mol / L CuSO 4 aqueous solution. Next, 0.02 g (3.3 × 10 -5 mol) of tetraphenylporphyrin (TPP) as a compound having a porphyrin-type skeleton, 0.02 g (3.3 × 10 -5 mol) of copper sulfate Aqueous solution of sodium carbonate and 0.032 g of sodium carbonate equivalent to copper sulfate to prevent corrosion of the reaction vessel, and the interior of the reaction vessel was purged with argon and sealed. Next, the reaction vessel was charged into the sand bath set at 350 C. The reaction temperature in the reaction vessel reached the reaction temperature in about 4 minutes.
  • 28
  • [ 917-23-7 ]
  • [ 91199-75-6 ]
  • [ 14172-91-9 ]
  • 29
  • [ 14172-91-9 ]
  • [ 68-12-2 ]
  • [ 71763-49-0 ]
YieldReaction ConditionsOperation in experiment
87% General procedure: Under the protection of nitrogen, 0.14 mmol of the corresponding 5,10,15,20-tetrakis(4-R-phenyl)porphyrin copper(II)complex was dissolved in 16 ml of CHCl3, to which 0.75 ml of DMFwas added with magnetic stirring. The solution was cooled to 0 Cin an ice bath, and then 0.56 ml of phosphoryl chloride (POCl3) wasslowly added within 20 min. The ice bath was removed and stirringwas continued at room temperature for 1 h, and the solution wascontinuously stirred and heated at 70 C for 24 h. Then 3.606 g ofNaAc and 14.4 ml of distilled water were added in an ice bath andstirring for another 1 h. After separation of the aqueous layer, theorganic layer was washed with 10 ml of distilled water for 3 times,then dried over anhydrous magnesium sulfate and filtered. Thesolvent was removed by rotary evaporation at low temperature toafford a crude product. The crude product was dissolved indichloromethane and subjected to column chromatography overneutral alumina with dichloromethane/petroleum ether (v/v 3:1)as the eluent. The third coloured bandwas collected and the solventwas removed by rotary evaporation to afford a purple powder.
  • 30
  • [ 14172-91-9 ]
  • [ 10544-72-6 ]
  • C44H28CuN6O4 [ No CAS ]
  • 31
  • [ 71147-55-2 ]
  • [ 124-41-4 ]
  • [ 14172-91-9 ]
  • [ 95386-81-5 ]
  • [ 95386-84-8 ]
  • 34
  • [ 10380-28-6 ]
  • N-methyl-5,10,15,20-tetraphenylporphyrin [ No CAS ]
  • [ 14172-91-9 ]
  • C45H31N4CuC9H6NO [ No CAS ]
  • 35
  • [ 14172-91-9 ]
  • (5,10,15,20-tetraphenylporphyrinato)copper(II) cation radical [ No CAS ]
  • 36
  • [ 14172-91-9 ]
  • copper(II) oxide [ No CAS ]
  • 40
  • [ 14172-91-9 ]
  • [ 293-42-5 ]
  • disulphidothionitrato(meso-tetraphenylporphyrinato)copper(III) [ No CAS ]
  • 42
  • [ 14172-91-9 ]
  • [ 123582-29-6 ]
  • 43
  • [ 14172-91-9 ]
  • copper(II) nitrate [ No CAS ]
  • [ 71147-55-2 ]
  • 44
  • [ 14172-91-9 ]
  • [ 131214-87-4 ]
YieldReaction ConditionsOperation in experiment
72% 0.0157 g (0.088 mmol) of N-bromosuccinimide was added to a solution of 0.04 g (0.059 mmol) of Cuin 20 mL of l3, and the mixture was refluxed during 30 min. The operation was repeated three times,total amount of the added N-bromosuccinimide being0.047 g (0.26 mmol). After addition of the last portion of the reactant, the mixture was refluxed during 2 hand cooled to ambient; a solution of 0.07 g (0.44 mmol)of bromine in 5 mL of CHCl3 was then added atstirring. The resulting mixture was kept at 20 during about 24 h. Excess of bromine was removed by washing the reaction mixture with 15 mL of 20%aqueous solution of Na2S2O3. The organic layer was washed with water and dried over Na2SO4. The solvent was removed, and the residue was purified by chromatographyon alumina eluting with chloroform,followed by recrystallization from ethanol. Yield 0.055 g(72%, 0.0421 mmol).
68% With N-Bromosuccinimide; In chloroform; N,N-dimethyl-formamide; at 20.0℃; for 8h; (a) N-Bromosuccinimide (0.105 g, 0.592 mmol) was added with stirring to a solution of 0.02 g (0.0296 mmol) of complex 5 in a mixture of 10 mL of chloroform and 1 mL of DMF, the mixture was stirred at ambient temperature for 8 h. The reaction mixture was concentrated to minimal volume, 10 mL of DMF, water, and solid NaCl were added, the precipitate was separated by filtration, washed with water, acetonitrile, dried, chromatographed on aluminum oxide using chloroform as an eluent, and reprecipitated from ethanol. Yield 0.026 g (0.0199 mmol), 68%. MS (m/z (Irel, %)): 1306.6 (98) [M]+; for C44H20N4Br8Cu calcd.: 1307.5. IR (nu, cm-1): 2925 s, 2853 m nu(C-H, Ph), 1680 w, 1488 m nu(C=C, Ph), 1467 w, 1444 w nu(C=N), 1366 w, 1351 w nu(C-N), 1175 m, 1145 w, 1108 w delta(C-H, Ph), 1024 s nu(C-C), 924 m, 858 m gamma(C-H, pyrrole ring), 756 m, 734 m, 695 m gamma(C-H, Ph). For C44H20N4Br8Cu anal. calcd. (%): C, 40.42; N, 4.29; H, 1.54; Br, 48.89. Found (%): C, 40.15; N, 4.16; H, 1.59; Br, 48.71.
  • 45
  • (N-methyl-5,10,15,20-tetraphenylporphinato)copper(II)(1+) [ No CAS ]
  • [ 111-92-2 ]
  • [ 1017265-92-7 ]
  • [ 14172-91-9 ]
  • 46
  • [ 14172-91-9 ]
  • [ 683-60-3 ]
  • copper(tetraphenylporphyrine) (1-) [ No CAS ]
  • 47
  • (N-methyl-5,10,15,20-tetraphenylporphinato)copper(II)(1+) [ No CAS ]
  • [ 109-89-7 ]
  • [ 14172-91-9 ]
  • [ 85649-95-2 ]
  • 48
  • [ 14172-91-9 ]
  • tris-(4-bromophenyl)aminium hexachloroantimonate [ No CAS ]
  • Cu(C6H5)4C20H8N4(1+)*SbCl6(1-) = {Cu(C6H5)4C20H8N4}SbCl6 [ No CAS ]
  • 49
  • copper(tetraphenylporphyrine) (1-) [ No CAS ]
  • [ 99685-96-8 ]
  • [ 14172-91-9 ]
  • fullerene [ No CAS ]
  • 50
  • [ 3524-08-1 ]
  • [ 14172-91-9 ]
  • 5,10,15,20-tetraphenylporphyrinatocopper(II)*4,6-dinitrobenzofuroxan [ No CAS ]
  • 51
  • [ 14172-91-9 ]
  • phenyloxathiinylium hexachloroantimonate [ No CAS ]
  • Cu(C20H8N4(C6H5)4)(1+)*SbCl6(1-)*0.5CH2Cl2={Cu(C20H8N4(C6H5)4)}{SbCl6}*0.5CH2Cl2 [ No CAS ]
  • 52
  • [ 553-26-4 ]
  • [ 14172-91-9 ]
  • [Cu(II)(tetraphenylporphyrin)(4,4'-bipyridine)2] [ No CAS ]
  • 53
  • [ 128-09-6 ]
  • [ 14172-91-9 ]
  • [ 873796-70-4 ]
  • 54
  • [ 917-23-7 ]
  • [ 31794-94-2 ]
  • [ 14172-91-9 ]
  • 55
  • [ 917-23-7 ]
  • Cu(AlaGly)Cl*H2O [ No CAS ]
  • [ 14172-91-9 ]
  • 56
  • [ 917-23-7 ]
  • Cu(AlaGly)*2H2O [ No CAS ]
  • [ 14172-91-9 ]
  • 57
  • [ 917-23-7 ]
  • [ 872605-81-7 ]
  • [ 14172-91-9 ]
  • 58
  • copper tetraphenylporphyrin o-xylene [ No CAS ]
  • [ 14172-91-9 ]
  • 59
  • [ 205876-11-5 ]
  • [ 14172-91-9 ]
  • 60
  • [ 14172-91-9 ]
  • 5-(4-fluoresceinpropyloxy)phenyl-10,15,20-triphenylporphyrin [ No CAS ]
  • [Cu((5,10,15,20-tetraphenylporphyrin))]*(C4H2NHCPh)(C4H2NCPh)C4H2NHCPh)(C4H2NCC6H4O(CH2)3OC13H6O(O)(C6H4COOH)) [ No CAS ]
  • 65
  • [ 917-23-7 ]
  • [CuCl2(adenine(+1H))2] [ No CAS ]
  • [ 14172-91-9 ]
  • 66
  • [ 14172-91-9 ]
  • [ 71-43-2 ]
  • [ 179032-09-8 ]
  • 67
  • [ 179032-09-8 ]
  • [ 14172-91-9 ]
  • 68
  • [ 14172-91-9 ]
  • [ 28132-68-5 ]
  • 70
  • [ 14977-07-2 ]
  • bis(acetylacetonate)copper(II) [ No CAS ]
  • [ 14172-91-9 ]
  • 71
  • [ 14172-91-9 ]
  • 2-Nitro-5,10,15,20-tetraphenylporphyrin [ No CAS ]
  • 72
  • [ 14172-91-9 ]
  • C56H34N8 [ No CAS ]
  • 73
  • [ 14172-91-9 ]
  • [ 1257333-46-2 ]
  • 74
  • [ 14172-91-9 ]
  • [ 1257333-47-3 ]
  • 75
  • [ 14172-91-9 ]
  • [ 1257333-49-5 ]
  • 76
  • [ 14172-91-9 ]
  • [ 1257333-50-8 ]
  • 77
  • [ 14172-91-9 ]
  • C56H32Br2Mg2N8 [ No CAS ]
  • 78
  • [ 14172-91-9 ]
  • [ 71147-55-2 ]
YieldReaction ConditionsOperation in experiment
84% With acetic anhydride; copper(II) nitrate; In chloroform; at 40.0℃; for 0.416667h; Weigh 5,10,15,20-tetraphenyl copper porphyrin 1.000 g (1.5 mmol) was dissolved in a three-necked flask containing 175 mL of chloroform and dissolved by electromagnetic stirring at 40 C,Then add 15 mL of acetic acid,40 mL of acetic anhydride, followed by addition of .28 g (1.5 mmol) of copper nitrate, the reaction was carried out for about 25 min. Thin layer chromatography was carried out until the feed point was almost disappeared, poured into 200 mL of ice water mixture, neutralized with sodium hydroxide solution to pH = 9, and then washed several times, dried with anhydrous sodium sulfate, standing for one hour, pumping, the filtrate was concentrated to saturation, add 30mL hot methanol recrystallization.The solid was washed with methanol to a colorless, dry, bright purple crystal, beta-nitro-5,10,15,20-tetraphenyl copper porphyrin 0.90 g, yield 84%.
  • 79
  • [ 14172-91-9 ]
  • 17,18-dioxo-5,10,15,20-tetraphenylchlorin [ No CAS ]
  • 80
  • [ 14977-07-2 ]
  • [ 14172-91-9 ]
  • 82
  • [ 14172-91-9 ]
  • [ 1334420-81-3 ]
  • 83
  • [ 14172-91-9 ]
  • 2-(1-acetyl-2-oxopropyl)-5,10,15,20-tetraphenylporphyrin [ No CAS ]
  • 84
  • [ 14172-91-9 ]
  • [ 1334420-82-4 ]
  • 86
  • [ 100-51-6 ]
  • [ 14172-91-9 ]
  • 87
  • [ 14172-91-9 ]
  • [ 437653-47-9 ]
  • 88
  • copper(II) nitrate trihydrate [ No CAS ]
  • [ 14172-91-9 ]
  • [ 71147-55-2 ]
YieldReaction ConditionsOperation in experiment
98% With acetic anhydride; acetic acid; In dichloromethane; at 20.0℃; for 3h;Inert atmosphere; General procedure: To a solution of corresponding porphyrin, the copper complex(1.13 mmol) in methylene chloride (90 mL) Cu(NO3)2·3H2O(2.30 mmol) in the mixture of acetic acid (5 mL) and acetic anhydride (2 mL) was added, and reaction mixture was stirred for 3 h at room temperature, with TLC monitoring (CHCl3-hexane 1:2). After completion of the reaction the solution was washed with water (200 mL), then with Na2CO3 solution, and the organic phase was separated and dried over Na2SO4. After removal of the solvent under reduced pressure, the residue was purified by column chromatography on silica gel using a CH2Cl2-hexane system (3:7).
89% With acetic acid; In chloroform; acetic anhydride; at 35.0℃; for 5h; Cu(II)TPP (3) (0.7 g, 1.0 mmol)was dissolved in chloroform (700 mL) and acetic acid (15 mL) was added. Cu(NO3)2·3H2O (0.63 g,2.6 mmol) was dissolved in acetic anhydride (70 mL) and added to the reaction mixture. The mixturewas heated to 35 C and let to stir for 5 h. The reaction mixture was washed with water(3 × 700 mL), saturated K2CO3 solution (2 × 700 mL) and again with water (2 × 700 mL), dried overanhydrous Na2SO4 and solvents removed by azeotropic evaporation with methanol. The residue waspurified by column chromatography using CH2Cl2:pentane 1:1 as eluent resulting in Cu(II)TPPNO2(4) as a dark purple solid (0.65 g, 0.89 mmol, 89%)
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