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Chemical Structure| 4282-46-6 Chemical Structure| 4282-46-6

Structure of 4282-46-6

Chemical Structure| 4282-46-6

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Product Details of [ 4282-46-6 ]

CAS No. :4282-46-6
Formula : C11H8N2O2
M.W : 200.19
SMILES Code : O=[N+](C1=CC=C(C2=CC=CN=C2)C=C1)[O-]
MDL No. :MFCD00276489

Safety of [ 4282-46-6 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319
Precautionary Statements:P501-P270-P264-P280-P302+P352-P337+P313-P305+P351+P338-P362+P364-P332+P313-P301+P312+P330

Application In Synthesis of [ 4282-46-6 ]

* 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 [ 4282-46-6 ]

[ 4282-46-6 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 7149-14-6 ]
  • [ 4282-46-6 ]
  • 2
  • [ 4282-46-6 ]
  • [ 19733-56-3 ]
YieldReaction ConditionsOperation in experiment
80.7% With hydrogenchloride; platinum(IV) oxide; hydrogen; In methanol; at 10 - 40℃; under 750.075 - 3000.3 Torr; for 18h; (20.0 g), methanol (180 mL) and 0.1 m hydrochloric acid are added to a hydrogenation reaction, and the reaction is carried out in the same manner as in the literature (Org. Process Res. Dev.2011, 15, 831-840). Specifically, 3- (4-nitrophenyl) Kettle, then add PtO2(2 g) was evacuated and the nitrogen was exchanged and the reaction mixture was cooled to 10 C2The reaction mixture was heated to 40 C, stirred for 18 h, cooled to room temperature, neutralized with sodium hydroxide solution, extracted with isopropyl acetate, concentrated, and added to the reaction mixture. The amount of N- (4- (pyridin-3-yl) phenyl) hydroxylamine was 4.2%
 

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