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Chemical Structure| 25351-89-7 Chemical Structure| 25351-89-7

Structure of 25351-89-7

Chemical Structure| 25351-89-7

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Product Details of [ 25351-89-7 ]

CAS No. :25351-89-7
Formula : C8H8N2O4
M.W : 196.16
SMILES Code : CC(NC1=CC=C([N+]([O-])=O)C=C1O)=O
MDL No. :MFCD00219839

Safety of [ 25351-89-7 ]

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 [ 25351-89-7 ]

* 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 [ 25351-89-7 ]

[ 25351-89-7 ] Synthesis Path-Downstream   1~2

  • 2
  • [ 25351-89-7 ]
  • [ 5683-43-2 ]
YieldReaction ConditionsOperation in experiment
85% With Amberlyst-15; In water; at 90℃; for 1.0h;Irradiation; General procedure: To a mixture of N-acyl or benzoy lderivative (6, 1 mmol) in water (5 mL) was added amberlyst-15 (10%, w/w) and the mixture was irradiated with ultrasound (40 KHz) continuously at 90 C till the completion of the reaction (monitored by TLC) as indicated in Table 4. The solid separated was filtered, washed with diethyl ether (2 x 5 mL), dried and treated with EtOAc (15 mL). After stirring for 10 min the mixture was filtered to remove the insoluble catalyst. The filtrate was collected and concentrated under vacuum. The solid obtained was purified by recrystallization (column chromatography in few cases) to afford the desired products 7, 8 or 9.
 

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