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[ CAS No. 37086-84-3 ] {[proInfo.proName]}

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Chemical Structure| 37086-84-3
Chemical Structure| 37086-84-3
Structure of 37086-84-3 * Storage: {[proInfo.prStorage]}
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Product Details of [ 37086-84-3 ]

CAS No. :37086-84-3 MDL No. :MFCD28363965
Formula : C10H12O3 Boiling Point : -
Linear Structure Formula :- InChI Key :-
M.W : 180.20 Pubchem ID :-
Synonyms :

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Application In Synthesis of [ 37086-84-3 ]

* 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 [ 37086-84-3 ]

[ 37086-84-3 ] Synthesis Path-Downstream   1~5

  • 1
  • [ 2568-25-4 ]
  • [ 36220-92-5 ]
  • [ 51591-52-7 ]
  • [ 7022-98-2 ]
  • [ 37086-84-3 ]
  • 3
  • [ 2568-25-4 ]
  • [ 6656-60-6 ]
  • [ 51591-52-7 ]
  • [ 37086-84-3 ]
  • 4
  • [ 57-55-6 ]
  • [ 93-97-0 ]
  • [ 37086-84-3 ]
YieldReaction ConditionsOperation in experiment
91% With tetrabutylammonium benzoate In acetonitrile at 40℃; Green chemistry; regioselective reaction; 4.2 General procedure for regioselective mono benzoylation General procedure: Diols and polyol reactants (100 mg) were allowed to react with benzoic anhydride (1.1 equiv) in acetonitrile (1 mL) at 40°C for 8-12 h in the presence of TBAOBz (0.2 equiv). The reaction mixture was directly purified by flash column chromatography (hexanes/EtOAc=2:1 to 1:1), affording the pure selectively protected derivatives.
90% With DBN In ethyl acetate at 40℃; Green chemistry; regioselective reaction;
85% With N-ethyl-N,N-diisopropylamine In acetonitrile at 40℃; Green chemistry; regioselective reaction;
80% With dmap; triethylamine In dichloromethane at 20℃;

  • 5
  • [ 644-32-6 ]
  • [ 57-55-6 ]
  • [ 37086-84-3 ]
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