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
Molecular Formula | C4H6O4 |
Molecular Weight | 118.088 |
Charge | 0 |
Count |
|
Stereochemistry | ACHIRAL |
Additional Stereochemistry | No |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Optical Activity | NONE |
Approval Year
PubMed
Title | Date | PubMed |
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Synthesis, structural evaluation, and estrogen receptor interaction of 2,3-diarylpiperazines. | 2002 May 23 |
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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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Metal-ligand-coordinated vesicles and vesicle-assisted preparation of calcium oxalate. | 2008 Feb 14 |
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Preparation of calcium oxalate by vesicle modification in the catanionic surfactant system CDS/TTABr/H2O. | 2010 Feb 18 |
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High activity and selectivity of Ag/SiO2 catalyst for hydrogenation of dimethyl oxalate. | 2010 Jun 28 |
|
The isolation of citric acid derivatives from Aspergillus niger. | 2010 May |
Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 02:01:38 GMT 2023
by
admin
on
Sat Dec 16 02:01:38 GMT 2023
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Record UNII |
IQ3Q79344S
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Record Status |
Validated (UNII)
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Record Version |
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553-90-2
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11120
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9374
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IQ3Q79344S
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DTXSID9060287
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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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PRIMARY | Merck Index | ||
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DIMETHYL OXALATE
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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
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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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