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Chemical Structure| 90770-88-0 Chemical Structure| 90770-88-0

Structure of 90770-88-0

Chemical Structure| 90770-88-0

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Product Details of [ 90770-88-0 ]

CAS No. :90770-88-0
Formula : C10H8N2O2
M.W : 188.18
SMILES Code : OC1=CC(C2=NC=CC(O)=C2)=NC=C1
MDL No. :MFCD08704189
InChI Key :JHDFNETXVFHWEE-UHFFFAOYSA-N
Pubchem ID :11789952

Safety of [ 90770-88-0 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H315-H319-H335
Precautionary Statements:P302+P352-P305+P351+P338

Application In Synthesis of [ 90770-88-0 ]

* 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 [ 90770-88-0 ]

[ 90770-88-0 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 17217-57-1 ]
  • [ 90770-88-0 ]
YieldReaction ConditionsOperation in experiment
91% With hydrogen bromide; acetic acid; In water; at 140℃;Inert atmosphere; To a solution of 4,4?-dimethoxy-2,2?-bipyridine (3.055 g, 14.13 mmol) in 180 ml of glacial acetic acid was added 48 wt percent HBr solution in water (25 ml, 146 mmol). The mixture was refluxed overnight at 140° C. under N2 (g). The mixture was allowed to cool and the solvent was removed in vacuo to render a white solid. The residue was dissolved in 100 ml of water and neutralised by adding aqueous ammonium hydroxide. The white solid (2.425 g, 12.89 mmol, 91percent yield) was filtered and dried, and used in the next step without further purification. 1H NMR (300 MHz, NaOD/D2O): deltaH=7.74 (s, 1H, OH), 7.38 (d, 2H, 3JH5=5.9 Hz, H6), 6.34 (d, 2H, 4JH5=2.4 Hz, H3), 5.85 (dd, 2H, 3JH6=5.9 Hz, 4JH3=2.4 Hz, H5). EI-MS(+): m/z 188.1 [M]+., 160.1 [M?N2)+., 94.0 [c-C5H3N?OH]+. IR (cm?1): 3209.17, 3059.21, 2760.30, 1594.48, 1523.34, 1475.20, 1393.46, 1218.35.
64% With hydrogen bromide; acetic acid;Reflux; The ligand was synthesized according to the literature with slight modifications. [2] HBr solution (41 wtpercent, 0.554 mL,2.77 mmol) was added to a mixture of glacial acetic acid (13.85 mL) and 4,4?-dimethoxy-2,2?-bipyridine (60 mg, 0.277 mmol); the resulting mixture was subsequently refluxed overnight. After cooling to room temperature, the solvent was removed under reduced pressure. The residue was dissolved in distilled water and neutralized to pH 6?7 by addition of aqueous ammonium hydroxide to provide a white precipitate with 64percent (33 mg) yield.
With hydrogen bromide; acetic acid; for 8h;Reflux; Specifically, 4,4'-Dimethoxy-2,2'-Bipyridine and HBr were refluxed with glacial acetic acid solvent for 6-10 hours. After completion of the reaction, neutralization was performed using ammonia water.
  • 2
  • [ 926-06-7 ]
  • [ 134179-43-4 ]
  • [ 90770-88-0 ]
  • 4-(tetra(ethyleneglycol)azido)-4'-isopropoxy-2,2'-bipyridine [ No CAS ]
  • C26H38N8O8 [ No CAS ]
  • C16H20N2O2 [ No CAS ]
 

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