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[ CAS No. 341556-86-3 ] {[proInfo.proName]}

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Chemical Structure| 341556-86-3
Chemical Structure| 341556-86-3
Structure of 341556-86-3 * Storage: {[proInfo.prStorage]}
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Product Details of [ 341556-86-3 ]

CAS No. :341556-86-3 MDL No. :MFCD06205370
Formula : C20H14O4 Boiling Point : -
Linear Structure Formula :- InChI Key :QGJNKGPCTYCXLD-WGDLNXRISA-N
M.W : 318.32 Pubchem ID :10734306
Synonyms :

Safety of [ 341556-86-3 ]

Signal Word:Warning Class:
Precautionary Statements:P261-P264-P271-P273-P280-P302+P352-P304+P340+P312-P305+P351+P338-P332+P313-P337+P313-P403+P233-P405-P501 UN#:
Hazard Statements:H315-H319-H335-H413 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 341556-86-3 ]

* 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 [ 341556-86-3 ]

[ 341556-86-3 ] Synthesis Path-Downstream   1~10

  • 1
  • [ 108366-06-9 ]
  • [ 341556-86-3 ]
YieldReaction ConditionsOperation in experiment
96% With potassium hydroxide In ethanol for 1h; Heating;
R.18 Reference Example 18 STR68 In a similar manner, 161 mg (96%) of 3,3'-(9,10-anthracenediyl)diacrylic acid was obtained from 200 mg (0.53 mmol) of ethyl 3,3'-(9,10-anthracenediyl)diacrylate. Melting point 310.5°-319.0° C. (decomposed) High resolution mass spectrum as C20 H14 O4; Calculated: 318.0892; Found: 318.0915
  • 2
  • (S)-8-Chloromethyl-4-hydroxy-2-trifluoromethyl-3,6,7,8-tetrahydro-pyrrolo[3,2-e]indole-1-carboxylic acid methyl ester; hydrochloride [ No CAS ]
  • [ 341556-86-3 ]
  • C48H34Cl2F6N4O8 [ No CAS ]
YieldReaction ConditionsOperation in experiment
25% With 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride In N,N-dimethyl-formamide at 20℃;
  • 3
  • [ 523-27-3 ]
  • [ 341556-86-3 ]
YieldReaction ConditionsOperation in experiment
Multi-step reaction with 2 steps 1: 94 percent / Et3N; 1,3-(diphenylphosphino)propane; Pd(OAc)2 / dimethylformamide / 10 h / 100 °C 2: 96 percent / KOH / ethanol / 1 h / Heating
YieldReaction ConditionsOperation in experiment
2 Example 2 STR30 To 13.5 mg (30 μmol) of methyl (S)-3-t-butoxycarbonyl-1-chloromethyl-5-hydroxy-7-trifluoromethyl-1,2,3,6-tetrahydropyrrolo[3,2-e]indole-8-carboxylate, was added 0.43 mL of 3M hydrogen chloride-ethyl acetate. The mixture was stirred at room temperature for 2 hours. Then the solvent was removed by distillation. The resulting residue was stirred with 4.8 mg (15 μmol) of 3,3'-(9,10-anthracenediyl)diacrylic acid and 17.3 mg (90 μmol) of 1-(3-dimethylaminopropyl) -3-ethylcarbodiimide hydrochloride in 0.3 mL of anhydrous dimethylformamide under an argon stream overnight. Water was added to the reaction mixture, and the resulting precipitate was purified by silica gel column chromatography (tetrahydrofuran:chloroform=2:1) to obtain 3.7 mg (25%) of (S,S)-3,3'-[3,3'-(9,10-anthracenediyl)diacryloyl]-bis›1-chloromethyl-5-hydroxy-7-trifluoromethyl-1,2,3,6-tetrahydropyrrolo [3,2-e]indole-8-methoxycarbonyl! in a yellow crystal state. [α]D29 =-144° (c=0.20, tetrahydrofuran); NMR (DMSO d6) δ: 3.56(2H,t,J=10 Hz), 3.79-3.85(2H,m), 3.87(6H,s), 4.22-4.29(2H,m), 4.33-4.47(4H,m), 7.05(2H,d,J=16 H) z), 7,66(4H,dd,J=4 and 7 Hz), 8.22(2H,s), 8.37(4H,dd,J=7 and 4 Hz), 8.55(2H,d,J=16 Hz), 10.64(2H,s), 13.11(2H,s).
  • 5
  • (2E,2'E)-dimethyl 3,3'-(anthracene-9,10-diyl)diacrylate [ No CAS ]
  • [ 341556-86-3 ]
YieldReaction ConditionsOperation in experiment
65.4% With water In tetrahydrofuran; methanol at 60℃; Alkaline conditions;
  • 6
  • barium(II) nitrate [ No CAS ]
  • [ 64-17-5 ]
  • [ 7732-18-5 ]
  • [ 33513-42-7 ]
  • [ 341556-86-3 ]
  • 5C20H12O4(2-)*5Ba(2+)*2C2H6O*3H2O*5C3H7NO [ No CAS ]
YieldReaction ConditionsOperation in experiment
70% at 30 - 90℃; for 66h; Sealed tube; High pressure;
  • 7
  • [ 33513-42-7 ]
  • lead(II) chloride [ No CAS ]
  • [ 341556-86-3 ]
  • [Pb(adda)(DMF)]n [ No CAS ]
YieldReaction ConditionsOperation in experiment
With water In ethanol at 90℃; for 72h; High pressure; 1-2 Example 1 Preparation of crystalline material [Pb(adda)(DMF)]n Put 0.15mmolPbCl2 and 0.15mmol (2E,2′E)-3,3′-(anthracen-9,10-diyl)diacrylic acid into a glass vial with a capacity of 20mL, Then a mixed solvent of 3 mL DMF, 2 mL ethanol and 1 mL water was added to perform a solvothermal reaction. The reaction temperature was 90° C., and the reaction time was 3 days. After the reaction, it was cooled to room temperature, filtered and washed to obtain yellow-green flake crystals [Pb(adda)(DMF)]n. Through X-ray single crystal diffraction analysis, the crystal was determined to be [Pb(adda)(DMF)]n.
  • 8
  • lead(II) nitrate [ No CAS ]
  • [ 33513-42-7 ]
  • [ 341556-86-3 ]
  • [Pb(adda)(DMF)]n [ No CAS ]
YieldReaction ConditionsOperation in experiment
With water In ethanol at 90℃; for 72h; High pressure; Example 1 Preparation of crystalline material [Pb(adda)(DMF)]n General procedure: Put 0.15mmolPbCl2 and 0.15mmol (2E,2′E)-3,3′-(anthracen-9,10-diyl)diacrylic acid into a glass vial with a capacity of 20mL, Then a mixed solvent of 3 mL DMF, 2 mL ethanol and 1 mL water was added to perform a solvothermal reaction. The reaction temperature was 90° C., and the reaction time was 3 days. After the reaction, it was cooled to room temperature, filtered and washed to obtain yellow-green flake crystals [Pb(adda)(DMF)]n. Through X-ray single crystal diffraction analysis, the crystal was determined to be [Pb(adda)(DMF)]n.
  • 9
  • [ 301-04-2 ]
  • [ 33513-42-7 ]
  • [ 341556-86-3 ]
  • [Pb(adda)(DMF)]n [ No CAS ]
YieldReaction ConditionsOperation in experiment
With water In ethanol at 120℃; for 72h; High pressure; Example 1 Preparation of crystalline material [Pb(adda)(DMF)]n General procedure: Put 0.15mmolPbCl2 and 0.15mmol (2E,2′E)-3,3′-(anthracen-9,10-diyl)diacrylic acid into a glass vial with a capacity of 20mL, Then a mixed solvent of 3 mL DMF, 2 mL ethanol and 1 mL water was added to perform a solvothermal reaction. The reaction temperature was 90° C., and the reaction time was 3 days. After the reaction, it was cooled to room temperature, filtered and washed to obtain yellow-green flake crystals [Pb(adda)(DMF)]n. Through X-ray single crystal diffraction analysis, the crystal was determined to be [Pb(adda)(DMF)]n.
  • 10
  • lead(II) bromide [ No CAS ]
  • [ 33513-42-7 ]
  • [ 341556-86-3 ]
  • [Pb(adda)(DMF)]n [ No CAS ]
YieldReaction ConditionsOperation in experiment
With water In ethanol at 100℃; for 72h; High pressure; Example 1 Preparation of crystalline material [Pb(adda)(DMF)]n General procedure: Put 0.15mmolPbCl2 and 0.15mmol (2E,2′E)-3,3′-(anthracen-9,10-diyl)diacrylic acid into a glass vial with a capacity of 20mL, Then a mixed solvent of 3 mL DMF, 2 mL ethanol and 1 mL water was added to perform a solvothermal reaction. The reaction temperature was 90° C., and the reaction time was 3 days. After the reaction, it was cooled to room temperature, filtered and washed to obtain yellow-green flake crystals [Pb(adda)(DMF)]n. Through X-ray single crystal diffraction analysis, the crystal was determined to be [Pb(adda)(DMF)]n.
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