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[ CAS No. 4702-32-3 ] {[proInfo.proName]}

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Chemical Structure| 4702-32-3
Chemical Structure| 4702-32-3
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Product Details of [ 4702-32-3 ]

CAS No. :4702-32-3 MDL No. :MFCD00005397
Formula : C6H6O6 Boiling Point : -
Linear Structure Formula :- InChI Key :UKZDIMBDWHZXOK-UHFFFAOYSA-N
M.W : 174.11 Pubchem ID :98259
Synonyms :

Safety of [ 4702-32-3 ]

Signal Word:Warning Class:N/A
Precautionary Statements:P261-P305+P351+P338 UN#:N/A
Hazard Statements:H315-H319-H335 Packing Group:N/A
GHS Pictogram:

Application In Synthesis of [ 4702-32-3 ]

* 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 [ 4702-32-3 ]

[ 4702-32-3 ] Synthesis Path-Downstream   1~5

  • 1
  • [ 320-77-4 ]
  • [ 4702-32-3 ]
YieldReaction ConditionsOperation in experiment
at 100℃;
  • 2
  • [ 4702-32-3 ]
  • [ 937-14-4 ]
  • [ 133191-92-1 ]
YieldReaction ConditionsOperation in experiment
15% With dicyclohexyl-carbodiimide In ethyl acetate at 0℃; for 0.25h;
YieldReaction ConditionsOperation in experiment
B. s. bei Isocitronensaeure, Bd. III, S. 555;
Mention may be made most particularly, alone or as a mixture, of the following lactones: ... 2-oxo-1-oxaspiro[4.5]decane-4-carboxylic acid 2-oxo-2H-pyran-3-carboxylic acid 4-methyl-2-oxo-2H-pyran-6-carboxylic acid 3-oxo-3H-naphtho[2,1-b]pyran-2-carboxylic acid tetrahydro-5-oxo-2,3-furandicarboxylic acid 1,3-dihydro-3-oxo-4-isobenzofurancarboxylic acid 1,3-dihydro-1-oxo-5-isobenzofurancarboxylic acid hexahydro-2-oxo-3,5-methano-2H-cyclopenta[b]furan-7-carboxylic acid ...
  • 4
  • [ 4702-32-3 ]
  • [ 908093-98-1 ]
  • (2RS,3SR)-2-diphenylmethoxycarbonyl-5-oxotetrahydrofuran-3-carboxylic acid [ No CAS ]
YieldReaction ConditionsOperation in experiment
In acetone R.3.1 (1) (1) Preparation of (2RS,3SR)-2-diphenylmethoxycarbonyl-5-oxotetrahydrofuran-3-carboxylic acid 262 mg of (2RS,3SR)-5-oxotetrahydrofuran-2,3-dicarboxylic acid in 5 ml of acetone was stirred with 291 mg of diphenyldiazomethane at room temperature for 20 minutes. The reaction solution was evaporated in vacuo to dryness. The residue was purified by silica gel column chromatography [chloroform/methanol=100/1→10/1] to give 163 mg of the title compound as a white powder.
In acetone R.4.1 (1) (1) Preparation of (2RS,3SR)-2-diphenylmethoxycarbonyl-5-oxotetrahydrofuran-3-carboxylic Acid 262 mg of (2RS,3SR)-5-oxotetrahydrofuran-2,3-dicarboxylic acid was dissolved in 5 ml of acetone, and 91 mg of diphenyldiazomethane was added thereto, followed by stirring at room temperature for 20 minutes. The reaction solution was evaporated to dryness under reduced pressure. The residue was purified by silica gel column chromatography (chloroform/methanol=100/1→10/1) to obtain 163 mg of the above-identified compound as white powder.
  • 5
  • [ 922-84-9 ]
  • [ 298-12-4 ]
  • [ 320-77-4 ]
  • [ 4702-32-3 ]
YieldReaction ConditionsOperation in experiment
In water at 50℃;
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