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Chemical Structure| 41175-50-2 Chemical Structure| 41175-50-2
Chemical Structure| 41175-50-2

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Synonyms: 8-Hydroxyjulolidine

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Product Details of 8-Hydroxyjulolidine

CAS No. :41175-50-2
Formula : C12H15NO
M.W : 189.25
SMILES Code : OC1=C2CCCN3CCCC(C=C1)=C23
Synonyms :
8-Hydroxyjulolidine
MDL No. :MFCD00006918
InChI Key :FOFUWJNBAQJABO-UHFFFAOYSA-N
Pubchem ID :170474

Safety of 8-Hydroxyjulolidine

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H315-H319-H335
Precautionary Statements:P261-P305+P351+P338

Application In Synthesis of 8-Hydroxyjulolidine

* 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 [ 41175-50-2 ]

[ 41175-50-2 ] Synthesis Path-Downstream   1~4

  • 3
  • [ 652-12-0 ]
  • [ 41175-50-2 ]
  • 9-(2-carboxy-3,4,5,6-tetrafluorobenzoyl)-8-hydroxyjulolidine [ No CAS ]
YieldReaction ConditionsOperation in experiment
63% In toluene; for 5h;Inert atmosphere; Reflux; Under a nitrogen atmosphere, added to toluene (10 mL) was a mixture of 8-hydroxyjulolidine (3.00 mmol, purchased from Wako Pure Chemical Industries, Ltd.) and <strong>[652-12-0]3,4,5,6-tetrafluorophthalic anhydride</strong> (compound (4-2), 3.00 mmol, purchased from Wako Pure Chemical Industries, Ltd.), followed by heating and refluxing them for five hours while performing stirring. After the reaction solution was cooled to room temperature, hexane was added thereto to collect an insoluble(s) by filtration. The insoluble(s) was dissolved in chloroform, and then purified by silica gel chromatography to obtain a compound (5-2) as a faint green solid. A yield was 63%. The reaction formula is shown below. Data of Compound (5-2): (0100) 400 MHz 1H-NMR (CDCl3/TMS) δ (ppm): 12.28 (1H, s), 6.49 (1H, s), 3.28 (4H, t), 2.71 (2H, t), 2.55 (2H, t), 1.92 (4H, m). (0101) HRMS (ESI) m/z calcd. for C20H14F4NO4 ([M-H]-): 408.0864, found: 408.0884.
  • 4
  • [ 41175-50-2 ]
  • [ 2737-22-6 ]
  • C31H28Br3N2O2(1+) [ No CAS ]
 

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