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Chemical Structure| 112078-00-9 Chemical Structure| 112078-00-9

Structure of 112078-00-9

Chemical Structure| 112078-00-9

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Product Details of [ 112078-00-9 ]

CAS No. :112078-00-9
Formula : C48H38Cl4N2O4
M.W : 848.64
SMILES Code : O=C1N(C2=C(C(C)C)C=CC=C2C(C)C)C(C3=CC(Cl)=C(C4=C(Cl)C=C5C(N(C6=C(C(C)C)C=CC=C6C(C)C)C(C7=CC(Cl)=C8C4=C75)=O)=O)C9=C8C(Cl)=CC1=C39)=O
MDL No. :N/A

Safety of [ 112078-00-9 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H315-H319-H335
Precautionary Statements:P261-P264-P271-P280-P302+P352-P304+P340-P305+P351+P338-P312-P362-P403+P233-P501

Application In Synthesis of [ 112078-00-9 ]

* 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 [ 112078-00-9 ]

[ 112078-00-9 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 539-15-1 ]
  • [ 112078-00-9 ]
  • 2,9-bis-(2,6-diisopropyl-phenyl)-5,6,12,13-tetrakis-[4-(2-dimethylamino-ethyl)-phenoxy]-anthra[2,1,9-<i>def</i>;6,5,10-<i>d</i>'<i>e</i>'<i>f</i>']diisoquinoline-1,3,8,10-tetraone [ No CAS ]
YieldReaction ConditionsOperation in experiment
With potassium carbonate; In 1-methyl-pyrrolidin-2-one; at 100℃; for 0.25h;Inert atmosphere; To a three-necked flask, 1.0 g (1.199 mmol) of Formula a, 828 mg (5.995 mmol) of K2CO3, and 990 mg (5.995 mmol) of Hordenine were added, followed by evacuating. Nitrogen was injected, and NMP was added thereto, followed by stirring. (0092) Then, the reactant was heated to 100 C. and stirred at the temperature for 15 minutes to finish the reaction. (0093) The reaction product was cooled to 25 C., hydrochloric acid was injected thereto, solid was filtered, and the solid thus filtered was washed with water. After that, the solid thus washed was dried in vacuum, and the dried solid was separated using column chromatography to obtain a compound represented by the following Formula 1-4. (0094) 1H NMR (CDCl3, 400 MHz): 8.165 (s, 4H), 7.447 (t, 2H), 7.312 (d, 4H), 7.308 (d, 8H), 7.012 (d, 8H), 2.848 (m, 12H), 2.470 (m, 8H), 2.248 (s, 24H), 1.077 (d, 24H)
With potassium carbonate; In 1-methyl-pyrrolidin-2-one; at 100℃; for 15h;Inert atmosphere; [0277] A three-necked flask was charged with 1.0 g of the compound a (1.199 mmol) and 828 mg of K2CO3 (5.995 mmol), 990 mg of Hordenine (Hordenine, 5.995 mmol) was added and hold it under vacuum , then after nitrogen was added, NMP was added and stirred. [0278] Next, after heating the temperature to 100 , the reaction was completed by stirring at this temperature for 15 hours. [0279] Next it was followed by cooling to 25 then , after adding hydrochloric acid, and after filtering the solid, the filtered solid was washed with water. The washed solid was vacuum dried, and the dried reaction product was subjected to column chromatography to obtain a compound represented by the following formula 2-4.
  • 2
  • [ 94-26-8 ]
  • [ 106-48-9 ]
  • [ 112078-00-9 ]
  • C77H63Cl3N2O10 [ No CAS ]
YieldReaction ConditionsOperation in experiment
68.7% After potassium carbonate (0.04 mol) was added to the solution of INT (0.04 mol) and N-methylpyrrolidone (266.1 g) produced in the above Production Example 1, the temperature was further raised to 120 C. In the above reaction solution, 4-butyl paraben (0.04 mol) was dissolved in N-methyl lylone (88.7 g) at 120 C for 2 hours. The solution formed in the solution. After maintaining the reaction at the same temperature for 1 hour, 4-chlorophenol (0.16 mol) and potassium carbonate (0.16 mol) were added, and stirring was carried out for 4 hours. The reaction solution was cooled to room temperature, and 3 L of distilled water was discharged. The resulting reddish-purple precipitate was filtered under reduced pressure and washed with methanol. After the filtrate was redissolved in dichloromethane (MC), it was filtered through cerium oxide to remove impurities, and recrystallized from hydrazine to collect a compound represented by Chemical Formula 3-7 in a yield of 68.7%.
68.7% The intermediate compound (0.04 mol) of the above Synthesis Example 2And N-methylpyrrolidone (266.1g) dissolved in potassium carbonate (0.04mol),The temperature was raised to 120 C.Paraben 4-butyl ester(0.04 mol) A liquid prepared by dissolving in N-methylpyrrolidone (88.7 g) was charged into the reaction solution at 120 C over 2 hours. After maintaining the reaction at the same temperature for 1 hour,4-chlorophenol (0.16 mol) and potassium carbonate (0.16 mol) were added, and stirring was maintained for 4 hours.The reaction solution was cooled to room temperature and discharged to 3 L of distilled water.The generated purple precipitate was filtered under reduced pressure, and washed with methanol.After the filtrate was dissolved in methylene chloride (MC) again,Filtered through silica to remove impurities, recrystallized with MeOH,The compound of Chemical Formula 3-7 was obtained in a yield of 68.7%.Solubility in PGMEA at 25 C is 3%
 

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