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Chemical Structure| 934687-48-6 Chemical Structure| 934687-48-6

Structure of 934687-48-6

Chemical Structure| 934687-48-6

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Product Details of [ 934687-48-6 ]

CAS No. :934687-48-6
Formula : C9H5ClN2O3
M.W : 224.60
SMILES Code : O=C1NC2=C(C=C([N+]([O-])=O)C=C2)C(Cl)=C1
MDL No. :MFCD12024334

Safety of [ 934687-48-6 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319-H335
Precautionary Statements:P261-P264-P270-P271-P280-P301+P312-P302+P352-P304+P340-P305+P351+P338-P330-P332+P313-P337+P313-P362-P403+P233-P405-P501

Application In Synthesis of [ 934687-48-6 ]

* 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 [ 934687-48-6 ]

[ 934687-48-6 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 20146-59-2 ]
  • [ 934687-48-6 ]
YieldReaction ConditionsOperation in experiment
97% With sulfuric acid; nitric acid; at 0℃; for 1h; A mixture of 4-chloro-1/-/-quinolin-2-one (from step 1 ; 17.8 g, 98.9 mmol) in sulfuric acid (52.7 mL, 989 mmol) was cooled to 0 C. Nitric acid (70%) (9.9 mL, 109 mmol) was added dropwise. The solution was stirred at 0 C for 1 h and then poured onto ice water. The yellow precipitate that formed was filtered and washed with water, methanol, ethyl acetate and diethyl ether before being stirred under vacuum at 120 C for approx. 10 min affording 4-chloro-6-nitroquinolin-2(1/-/)-one (21.5 g, 97%) as a pale yellow solid. LCMS (Method T2) RT 1.27 min; m/z 225.01 [M+H]+.
21.5 g With sulfuric acid; nitric acid; at 0℃; for 1h; A mixture of 4-chloro-1 H-quinolin-2-one (17.8 g, 98.9 mmol) in sulfuric acid (52.7 mL, 989 mmol) was cooled to 0 00. Nitric acid (70%) (9.90 mL, 109 mmol) was added dropwise. The solution was stirred at 0 00 for 1 h and then poured onto ice water. The yellow precipitate that formed was filtered and washed with water, methanol, ethyl acetate and diethyl ether before being stirred under vacuum at 120 00 for -10 mins affording 4-chloro-6-nitro-1H- quinolin-2-one (21.5 g) as a pale yellow solid. LCMS (Method T2) Rt = 1.27 mins, mlz 225.01 [M+H]+.
 

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