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[ CAS No. 47593-50-0 ] {[proInfo.proName]}

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Chemical Structure| 47593-50-0
Chemical Structure| 47593-50-0
Structure of 47593-50-0 * Storage: {[proInfo.prStorage]}
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Product Details of [ 47593-50-0 ]

CAS No. :47593-50-0 MDL No. :MFCD00625984
Formula : C22H18O6 Boiling Point : -
Linear Structure Formula :- InChI Key :AYEXKJKXZHOWPW-UHFFFAOYSA-N
M.W : 378.37 Pubchem ID :1204453
Synonyms :

Safety of [ 47593-50-0 ]

Signal Word:Warning Class:N/A
Precautionary Statements:P264-P280-P302+P352-P337+P313-P305+P351+P338-P362+P364-P332+P313 UN#:N/A
Hazard Statements:H315-H319 Packing Group:N/A
GHS Pictogram:

Application In Synthesis of [ 47593-50-0 ]

* 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 [ 47593-50-0 ]

[ 47593-50-0 ] Synthesis Path-Downstream   1~11

  • 1
  • [ 938463-77-5 ]
  • [ 47593-50-0 ]
  • [ 5743-04-4 ]
  • Cd(1,4-bis(2-(pyridin-2-yl)-1H-imidazol-1-yl)butane)0.5(4,4'-(1,4-phenylenebis(methylene))bis(oxy)dibenzoate)) [ No CAS ]
YieldReaction ConditionsOperation in experiment
74% With NaOH In water High Pressure; mixt. of 1,4-bis(2-(pyridin-2-yl)-1H-imidazol-1-yl)butane, ligand, Cd(CH3CO2)2*2H2O, NaOH, H2O stirred for 1 h, sealed in autoclave, heated at 150°C for 72 h, cooled to 100°C at 10°C/h, held for 8 h, cooled to 30°C; collected; elem. anal.;
  • 2
  • zinc(II) sulfate heptahydrate [ No CAS ]
  • [ 4916-57-8 ]
  • [ 47593-50-0 ]
  • [Zn(4,4′-[1,4-phenylenebis(methylene)]bis(oxy)}dibenzoic acid(-2H))(1,2-bis(4-pyridyl)ethane)0.5] [ No CAS ]
YieldReaction ConditionsOperation in experiment
60% In water; N,N-dimethyl-formamide at 145℃; for 48h; High pressure;
  • 3
  • zinc(II) sulfate heptahydrate [ No CAS ]
  • [ 17252-51-6 ]
  • [ 47593-50-0 ]
  • [ 7732-18-5 ]
  • Zn(5,5′-phenylenebis(methylene)-1,1′-3,3′-(benzene-tetracarboxylic acid)(-4H))0.5-(1,3-bis(4-pyridyl)-propane)(H2O) [ No CAS ]
YieldReaction ConditionsOperation in experiment
60% In N,N-dimethyl-formamide at 145℃; for 48h; High pressure;
  • 4
  • zinc(II) sulfate heptahydrate [ No CAS ]
  • [ 17252-51-6 ]
  • [ 47593-50-0 ]
  • [Zn(4,4′-[1,4-phenylenebis(methylene)]bis(oxy)}dibenzoic acid(-2H))(1,3-bis(4-pyridyl)-propane)] [ No CAS ]
YieldReaction ConditionsOperation in experiment
40% In water; N,N-dimethyl-formamide at 145℃; for 48h; High pressure;
  • 5
  • [ 855766-92-6 ]
  • zinc(II) sulfate heptahydrate [ No CAS ]
  • [ 47593-50-0 ]
  • [ 7732-18-5 ]
  • [Zn(5,5′-phenylenebis(methylene)-1,1′-3,3′-(benzene-tetracarboxylic acid)(-2H))(4,4′-di(1H-imidazol-1-yl)-1,1′-biphenyl)]·H2O [ No CAS ]
YieldReaction ConditionsOperation in experiment
48% In N,N-dimethyl-formamide at 145℃; for 48h; High pressure;
  • 6
  • [ 855766-92-6 ]
  • zinc(II) sulfate heptahydrate [ No CAS ]
  • [ 47593-50-0 ]
  • [Zn(4,4′-[1,4-phenylenebis(methylene)]bis(oxy)}dibenzoic acid(-H))2(4,4′-di(1H-imidazol-1-yl)-1,1′-biphenyl)2] [ No CAS ]
YieldReaction ConditionsOperation in experiment
45% In water; N,N-dimethyl-formamide at 145℃; for 48h; High pressure;
  • 7
  • zinc(II) sulfate heptahydrate [ No CAS ]
  • [ 47593-50-0 ]
  • [ 7732-18-5 ]
  • [ 69506-92-9 ]
  • [Zn(5,5′-phenylenebis(methylene)-1,1′-3,3′-(benzene-tetracarboxylic acid)(-4H))0.5(1,3-bis((1H-imidazol-l-yl)methyl)-benzene)]·H2O [ No CAS ]
YieldReaction ConditionsOperation in experiment
50% In N,N-dimethyl-formamide at 145℃; for 48h; High pressure;
  • 8
  • zinc(II) sulfate heptahydrate [ No CAS ]
  • [ 47593-50-0 ]
  • [ 56643-83-5 ]
  • [ 7732-18-5 ]
  • [Zn(4,4′-[1,4-phenylenebis(methylene)]bis(oxy)}dibenzoic acid(-2H))-(1,4-bis((1H-imidazol-l-yl)methyl)benzene)]·H2O [ No CAS ]
YieldReaction ConditionsOperation in experiment
52% In N,N-dimethyl-formamide at 145℃; for 48h; High pressure;
  • 9
  • [ 4204-63-1 ]
  • [ 47593-50-0 ]
YieldReaction ConditionsOperation in experiment
85% With potassium hydroxide In methanol; water at 80℃; for 12h; Inert atmosphere;
  • 10
  • europium(III) chloride hexahydrate [ No CAS ]
  • [ 47593-50-0 ]
  • [ 7732-18-5 ]
  • Eu(PMBB)<SUB>1.5</SUB>(H<SUB>2</SUB>O)<SUB>2</SUB> [ No CAS ]
YieldReaction ConditionsOperation in experiment
72% With hydrogenchloride; N,N-dimethyl acetamide at 120℃; for 24h; Autoclave; 2.2. Preparation of complexes Ln-MOF General procedure: LnCl 3*6H 2 O, (0.1 mmol), H 2 PMBB (0.045 g, 0.12 mmol), H 2 O (10 mL), DMA (10 mL) and HCl (1 M, 3 mL) were placed in a 25 mL Teflon-lined stainless-steel autoclave, and the resulted sus- pension was heated at 120 °C for 1 d. Furthermore, the autoclave was placed at room temperature. Colorless prism crystals appropri- ate for single crystal X-ray diffraction analysis were collected from the precipitation of reaction solution. The final reaction system was filtrated, and the solids were rinsed several times with H 2 O and methanol, and dried in air at ambient temperature. EuCl 3 ·6H 2 O (0.037 g), yield, 72% (based on Eu III ); IR (neat): 1601 (s), 1586 (s), 1532 (s), 1422 (s), 1387 (s), 1372 (s), 1293 (s), 1241 (s), 1174 (s), 1146 (s), 1100 (s), 1006 (s), 874 (s), 846 (s), 800 (s), 782 (s), 695 (s), 639 (s), 630 (s), 550 (s), 531 (s) cm -1 ; element analysis (%): calcd. for C 33 H 28 O 11 Eu: C 52.67, H 3.75; found: C 53.01, H 3.80.
  • 11
  • [ 47593-50-0 ]
  • terbium(III) chloride hexahydrate [ No CAS ]
  • [ 7732-18-5 ]
  • Tb(PMBB)<SUB>1.5</SUB>(H<SUB>2</SUB>O)<SUB>2</SUB> [ No CAS ]
YieldReaction ConditionsOperation in experiment
76% With hydrogenchloride; N,N-dimethyl acetamide at 120℃; for 24h; Autoclave; 2.2. Preparation of complexes Ln-MOF General procedure: LnCl 3*6H 2 O, (0.1 mmol), H 2 PMBB (0.045 g, 0.12 mmol), H 2 O (10 mL), DMA (10 mL) and HCl (1 M, 3 mL) were placed in a 25 mL Teflon-lined stainless-steel autoclave, and the resulted sus- pension was heated at 120 °C for 1 d. Furthermore, the autoclave was placed at room temperature. Colorless prism crystals appropri- ate for single crystal X-ray diffraction analysis were collected from the precipitation of reaction solution. The final reaction system was filtrated, and the solids were rinsed several times with H 2 O and methanol, and dried in air at ambient temperature.
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