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[ CAS No. 33900-62-8 ] {[proInfo.proName]}

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Chemical Structure| 33900-62-8
Chemical Structure| 33900-62-8
Structure of 33900-62-8 * Storage: {[proInfo.prStorage]}
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Product Details of [ 33900-62-8 ]

CAS No. :33900-62-8 MDL No. :MFCD00238585
Formula : C10H14O4 Boiling Point : -
Linear Structure Formula :- InChI Key :-
M.W : 198.22 Pubchem ID :-
Synonyms :

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Application In Synthesis of [ 33900-62-8 ]

* 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 [ 33900-62-8 ]

[ 33900-62-8 ] Synthesis Path-Downstream   1~5

  • 1
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  • [ 14059-92-8 ]
  • 4
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  • [ 530-55-2 ]
YieldReaction ConditionsOperation in experiment
72% With C44H60CoN4O2(2+); oxygen In methanol at 0℃; for 16h; Inert atmosphere;
56% With nitric acid; sodium nitrite In methanol at -20℃;
With C52H68CoN6O2; oxygen In methanol at 20℃; for 16h; Sealed tube; 4.2. General procedure for the oxidation of lignin models General procedure: CAUTION: The oxidation reactions were performed in thick-walled, glass Fisher-Porter tubes under pressurized oxygen. Though no difficulties were experienced, adequate precautions should be considered when using organic compounds and oxygen above atmospheric pressure. Lignin models were oxidized according to a previously published procedure [19,30]. Briefly, to a Fisher-Porter tube was added 1 equivalent of the lignin model, 0.05 equivalents of Co-Schiff base catalyst, and the appropriate amount of methanol or dichloromethane to make a 0.2 M solution relative to the lignin model substrate. The tube was flushed three times and then pressurized to 50 psi using oxygen. Once pressurized, the reaction was stirred at room temperature for times denoted in Tables 1-3. If significant quantities of yellow solid (quinone) precipitated upon completion of the reaction, the mixture was filtered, and the mother liquor was concentrated under reduced pressure. This residue was analyzed by NMR to determine the amount of any additional quinone. If minimal or no yellow solid was present upon completion of the reaction, the mixture was concentrated under reduced pressure. Purification (silica gel; 0-2-5-10-100%EtOAc:DCM) gave the respective para-benzoquinones in yields reported in Tables 1-3.
  • 5
  • [ 33900-62-8 ]
  • [ 2478-38-8 ]
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