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Chemical Structure| 19414-67-6 Chemical Structure| 19414-67-6

Structure of 19414-67-6

Chemical Structure| 19414-67-6

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Product Details of [ 19414-67-6 ]

CAS No. :19414-67-6
Formula : C48H36N4Zn
M.W : 734.24
SMILES Code : CC(C=C1)=CC=C1C(C2=CC=C3C(C4=CC=C(C)C=C4)=C5C=CC(C(C6=CC=C(C)C=C6)=C7C=C8)=[N]95)=C%10C=CC%11=[N]%10[Zn+2]9([N-]23)[N-]7C8=C%11C%12=CC=C(C)C=C%12

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Application In Synthesis of [ 19414-67-6 ]

* 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 [ 19414-67-6 ]

[ 19414-67-6 ] Synthesis Path-Downstream   1~3

  • 1
  • [ 14527-51-6 ]
  • [ 19414-67-6 ]
  • 2
  • [ 557-34-6 ]
  • [ 14527-51-6 ]
  • [ 19414-67-6 ]
YieldReaction ConditionsOperation in experiment
59 mg In tetrahydrofuran; methanol; at 65℃; for 1.5h;Inert atmosphere; Dissolve 67 mg of <strong>[14527-51-6]TTP</strong> (that is, R5 = R6 = R7 = R8 = methyl in formula (III)) in 15 mL of tetrahydrofuran solution, and add 36 mg of zinc acetate in 5 mL of methanol to the above solution; Blow in nitrogen to remove the air in the system, then under the protection of a nitrogen ball, heat and stir at 65C, monitor the progress of the reaction by UV, and stop the reaction after 1.5h. Add 50 mL of ice water to the reaction system, refrigerate overnight, and then suction and filter to obtain 89 mg of brown-red solid powder; The resulting solid product was dissolved in chloroform, separation and purification by gel column chromatography, the mobile phase used is methanol, a purified product is obtained; then after the purified product is dissolved in chloroform, the precipitate was dissolved in chloroform and separated by silica gel column chromatography (developing solvent chloroform: methanol =5:1) to obtain 59 mg of product.
  • 3
  • [ 14527-51-6 ]
  • [ 7646-85-7 ]
  • [ 19414-67-6 ]
YieldReaction ConditionsOperation in experiment
In methanol; water; 67 g (1 mol) of pyrrol was reflux-boiled with 92 g (1 mol) of 4-methylbenzaldehyde in 400 ml of methanol+20 ml conc. HCl in a nitrogen atmosphere for 1 hour, whereby a dark blue solution of tetratolyl porphyrine was spontaneously obtained. After adding 136 g (1 mol) of zinc chloride, a suspension of the porphyrine zinc complex was obtained.
 

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