Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C3H4O6 |
| Molecular Weight | 136.0603 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
OC(=O)C(O)(O)C(O)=O
InChI
InChIKey=VUCKYGJSXHHQOJ-UHFFFAOYSA-N
InChI=1S/C3H4O6/c4-1(5)3(8,9)2(6)7/h8-9H,(H,4,5)(H,6,7)
| Molecular Formula | C3H4O6 |
| Molecular Weight | 136.0603 |
| 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 |
|---|---|---|
| [Cu3(Hmesox)3]3-: a precursor for the rational design of chiral molecule-based magnets (H4mesox = 2-dihydroxymalonic acid). | 2010-09-06 |
|
| Tetrahydroxy-p-benzoquinone as a source of polydentate O-donor ligands. Synthesis, crystal structure, and magnetic properties of the [Cu(bpy)(dhmal)]2 dimer and the two-dimensional [{SiW12O40}{Cu2(bpy)2(H2O)(ox)}2].16H2O inorganic-metalorganic hybrid. | 2007-02-19 |
|
| Pyrophosphate analogues as inhibitors of herpes simplex virus type 1 DNA polymerase. | 1980-03-28 |
Patents
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 21:19:21 GMT 2025
by
admin
on
Mon Mar 31 21:19:21 GMT 2025
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| Record UNII |
OT429C180H
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| Record Status |
Validated (UNII)
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| Record Version |
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| Code System | Code | Type | Description | ||
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DIHYDROXYMALONIC ACID
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68412
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209-208-8
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DTXSID70905078
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m7253
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OT429C180H
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560-27-0
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