Details
Stereochemistry | ACHIRAL |
Molecular Formula | C4H6O4 |
Molecular Weight | 118.088 |
Optical Activity | NONE |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
COC(=O)C(=O)OC
InChI
InChIKey=LOMVENUNSWAXEN-UHFFFAOYSA-N
InChI=1S/C4H6O4/c1-7-3(5)4(6)8-2/h1-2H3
Approval Year
PubMed
Title | Date | PubMed |
---|---|---|
Synthesis, structural evaluation, and estrogen receptor interaction of 2,3-diarylpiperazines. | 2002 May 23 |
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Preparation of enantiopure biimidazoline ligands and their use in asymmetric catalysis. | 2004 Jul 21 |
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Selectivity control of carbonylation of methanol to dimethyl oxalate and dimethyl carbonate over gold anode by electrochemical potential. | 2004 May 5 |
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Active control of methanol carbonylation selectivity over Au/carbon anode by electrochemical potential. | 2005 May 12 |
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Host-guest interaction in a thiourea-dimethyl oxalate (2/1) complex at 300 and 100 K. | 2006 Sep |
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High activity and selectivity of Ag/SiO2 catalyst for hydrogenation of dimethyl oxalate. | 2010 Jun 28 |
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The isolation of citric acid derivatives from Aspergillus niger. | 2010 May |
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553-90-2
Created by
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11120
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9374
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IQ3Q79344S
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DTXSID9060287
Created by
admin on Sat Dec 16 02:01:38 GMT 2023 , Edited by admin on Sat Dec 16 02:01:38 GMT 2023
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m7449
Created by
admin on Sat Dec 16 02:01:38 GMT 2023 , Edited by admin on Sat Dec 16 02:01:38 GMT 2023
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DIMETHYL OXALATE
Created by
admin on Sat Dec 16 02:01:38 GMT 2023 , Edited by admin on Sat Dec 16 02:01:38 GMT 2023
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209-053-6
Created by
admin on Sat Dec 16 02:01:38 GMT 2023 , Edited by admin on Sat Dec 16 02:01:38 GMT 2023
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SUBSTANCE RECORD