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Chemical Structure| 10342-60-6 Chemical Structure| 10342-60-6

Structure of 10342-60-6

Chemical Structure| 10342-60-6

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Product Details of [ 10342-60-6 ]

CAS No. :10342-60-6
Formula : C10H13NO2
M.W : 179.22
SMILES Code : O=[N+](C1=CC=C(CC(C)C)C=C1)[O-]
MDL No. :MFCD00130032
Boiling Point : No data available

Safety of [ 10342-60-6 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H315-H319-H335-H413
Precautionary Statements:P261-P264-P271-P273-P280-P302+P352-P304+P340+P312-P305+P351+P338-P332+P313-P337+P313-P403+P233-P405-P501

Application In Synthesis of [ 10342-60-6 ]

* 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 [ 10342-60-6 ]

[ 10342-60-6 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 538-93-2 ]
  • [ 19370-33-3 ]
  • [ 10342-60-6 ]
  • 2
  • [ 538-93-2 ]
  • [ 19370-33-3 ]
  • [ 10342-60-6 ]
  • 3-Isobutyl-nitrobenzol [ No CAS ]
YieldReaction ConditionsOperation in experiment
With bismuth(lll) trifluoromethanesulfonate; dinitrogen pentoxide; In dichloromethane; at 0℃; for 2.0h;Green chemistry; General procedure: In order to show the generality and scope of this new protocol,a range of simple aromatic compounds were treatedwith 1 equiv. of dinitrogen pentoxide in dichloromethane at0 C in the presence of 4 mol% Bi(OTf)3. The results aresummarized in (Table 3). In most cases, complete nitrationwas observed within 2 h, and the products were readily isolatedin near quantitative yields. For the deactivated aromaticring (R=NO2), incomplete nitration was observed at 0 C.Conducting these reactions at slightly elevated temperatures(30 C) resulted in a higher yield of nitrated products. Thesereaction conditions are extremely mild, and dinitration wasnot observed in all reactions.
 

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