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Chemical Structure| 1152844-08-0 Chemical Structure| 1152844-08-0

Structure of 1152844-08-0

Chemical Structure| 1152844-08-0

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Product Details of [ 1152844-08-0 ]

CAS No. :1152844-08-0
Formula : C8H8N4O3
M.W : 208.17
SMILES Code : O=[N+](C1=CC=C(OC)C(CN=[N+]=[N-])=C1)[O-]
MDL No. :MFCD11637176

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Application In Synthesis of [ 1152844-08-0 ]

* 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 [ 1152844-08-0 ]

[ 1152844-08-0 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 3913-23-3 ]
  • [ 1152844-08-0 ]
YieldReaction ConditionsOperation in experiment
80% With sodium azide; In N,N-dimethyl-formamide; at 20℃; for 12h; Step 2: Synthesis of 2-(azidomethyl)-l-methoxy-4-nitrobenzene (3); 2-(bromomethyl)-l -methoxy-4-nitrobenzene (2, 0.2 g, 0.8128 mmol) was taken up in DMF (2 mL) to form a mixture, sodium azide (52 mg, 0.8128 mmol) was added to the mixture, and the mixture was stirred at room temperature for 12 h. The progress of the reaction was monitored by TLC and liquid chromtography-mass spectrometry (LCMS). After completion of the reaction, water was added and the product was extracted with ethyl acetate. The combined organic extracts were washed with brine, dried over anhydrous sodium sulfate and concentrated under reduced pressure to afford 2-(azidomethyl)-l - methoxy-4-nitrobenzene (3, 0.161 g, 80 %), which was used in the next step without further purification. NMR (400 MHz, CDCI3): delta 8.30-8.20 (m, 2H), 7.00-6.95 (d, 1 H), 4.44 (s, 2H), 4.02 (s, 3H).
 

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