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Chemical Structure| 28232-35-1 Chemical Structure| 28232-35-1

Structure of 28232-35-1

Chemical Structure| 28232-35-1

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Product Details of [ 28232-35-1 ]

CAS No. :28232-35-1
Formula : C12H10N2O3
M.W : 230.22
SMILES Code : O=[N+](C1=CC=C(OC2=CC=CC=C2)N=C1C)[O-]
MDL No. :MFCD28991939

Safety of [ 28232-35-1 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H320-H335
Precautionary Statements:P261-P280-P301+P312-P302+P352-P305+P351+P338

Application In Synthesis of [ 28232-35-1 ]

* 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 [ 28232-35-1 ]

[ 28232-35-1 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 22280-60-0 ]
  • [ 108-95-2 ]
  • [ 28232-35-1 ]
YieldReaction ConditionsOperation in experiment
97% With caesium carbonate; In acetonitrile; at 0 - 20℃; for 15h; A round bottom flask containing 6-chloro-2- methyl-3-nitropyridine (50.1 g, 290 mmol) and CH3CN (230 mL) was cooled at 0 °C. Phenol (41.0 g, 436 mmol) was added followed by Cs2C03 (148 g, 454 mmol). The reaction mixture was allowed to warm to room temperature and stirred for 15 h. The mixture was transferred to a 2L Erlenmeyer flask, then diluted with water to a total volume of 1.8 L. The resulting suspension was stirred at room temperature for 10 min, then the solid was isolated by filtration, rinsed with water and dried to yield the title compound (64.7 g, 97percent yield) as a brown solid. MS (ESI): mass calcd. for ci2Hi0N2O3, 230.07; m/z found, 231.0 [M+H]+
97% With caesium carbonate; In acetonitrile; at 0 - 20℃; for 15h; A round bottom flask containing <strong>[22280-60-0]6-chloro-2-methyl-3-nitropyridine</strong> (50.1 g, 290 mmol) and CH 3CN (230 mL) was cooled at 0 . Phenol (41.0 g, 436 mmol) was added followed by Cs 2CO 3 (148 g, 454 mmol). The reaction mixture was allowed to warm to room temperature and stirred for 15 h. The mixture was transferred to a 2L Erlenmeyer flask, then diluted with water to a total volume of 1.8 L. The resulting suspension was stirred at room temperature for 10 min, then the solid was isolated by filtration, rinsed with water and dried to yield the title compound (64.7 g, 97percent yield) as a brown solid. MS (ESI) : mass calcd. for C 12H 10N 2O 3, 230.07 m/z found, 231.0 [M+H] +
 

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