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 |
|---|---|---|
| High activity and selectivity of Ag/SiO2 catalyst for hydrogenation of dimethyl oxalate. | 2010-06-28 |
|
| The isolation of citric acid derivatives from Aspergillus niger. | 2010-05 |
|
| Catalytic properties of [Pd(COOMe)(n)X(2-n)(PPh(3))(2)] (n = 0, 1, 2; X = Cl, NO(2), ONO(2), OAc and OTs) in the oxidative carbonylation of MeOH. | 2010-04-19 |
|
| Preparation of calcium oxalate by vesicle modification in the catanionic surfactant system CDS/TTABr/H2O. | 2010-02-18 |
|
| Novel C2-symmetric macrocycles bearing diamide-diester groups: synthesis and enantiomeric recognition for primary alkyl ammonium salts. | 2008-04-04 |
|
| Metal-ligand-coordinated vesicles and vesicle-assisted preparation of calcium oxalate. | 2008-02-14 |
|
| Host-guest interaction in a thiourea-dimethyl oxalate (2/1) complex at 300 and 100 K. | 2006-09 |
|
| A tripodal sulfur ligand for the selective ruthenium-catalysed hydrogenation of dimethyl oxalate. | 2006-06-04 |
|
| Synthesis of nitrogen and sulfur macrocycles with cis exogenous oxygen and sulfur donor atoms. | 2005-12-07 |
|
| Active control of methanol carbonylation selectivity over Au/carbon anode by electrochemical potential. | 2005-05-12 |
|
| Preparation of enantiopure biimidazoline ligands and their use in asymmetric catalysis. | 2004-07-21 |
|
| Selectivity control of carbonylation of methanol to dimethyl oxalate and dimethyl carbonate over gold anode by electrochemical potential. | 2004-05-05 |
|
| Synthesis, structural evaluation, and estrogen receptor interaction of 2,3-diarylpiperazines. | 2002-05-23 |
| Name | Type | Language | ||
|---|---|---|---|---|
|
Official Name | English | ||
|
Preferred Name | English | ||
|
Common Name | English | ||
|
Code | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Common Name | English |
| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
|
553-90-2
Created by
admin on Mon Mar 31 21:06:45 GMT 2025 , Edited by admin on Mon Mar 31 21:06:45 GMT 2025
|
PRIMARY | |||
|
11120
Created by
admin on Mon Mar 31 21:06:45 GMT 2025 , Edited by admin on Mon Mar 31 21:06:45 GMT 2025
|
PRIMARY | |||
|
9374
Created by
admin on Mon Mar 31 21:06:45 GMT 2025 , Edited by admin on Mon Mar 31 21:06:45 GMT 2025
|
PRIMARY | |||
|
IQ3Q79344S
Created by
admin on Mon Mar 31 21:06:45 GMT 2025 , Edited by admin on Mon Mar 31 21:06:45 GMT 2025
|
PRIMARY | |||
|
DTXSID9060287
Created by
admin on Mon Mar 31 21:06:45 GMT 2025 , Edited by admin on Mon Mar 31 21:06:45 GMT 2025
|
PRIMARY | |||
|
m7449
Created by
admin on Mon Mar 31 21:06:45 GMT 2025 , Edited by admin on Mon Mar 31 21:06:45 GMT 2025
|
PRIMARY | Merck Index | ||
|
DIMETHYL OXALATE
Created by
admin on Mon Mar 31 21:06:45 GMT 2025 , Edited by admin on Mon Mar 31 21:06:45 GMT 2025
|
PRIMARY | |||
|
209-053-6
Created by
admin on Mon Mar 31 21:06:45 GMT 2025 , Edited by admin on Mon Mar 31 21:06:45 GMT 2025
|
PRIMARY |
SUBSTANCE RECORD
