Details
| Stereochemistry | RACEMIC |
| Molecular Formula | C6H10O3 |
| Molecular Weight | 130.1418 |
| Optical Activity | ( + / - ) |
| Defined Stereocenters | 0 / 1 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CCOC(C)C(=O)C=O
InChI
InChIKey=VUNAKDMJSGEODG-UHFFFAOYSA-N
InChI=1S/C6H10O3/c1-3-9-5(2)6(8)4-7/h4-5H,3H2,1-2H3
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Synthesis, cytotoxic activity, and DNA binding properties of copper (II) complexes with hesperetin, naringenin, and apigenin. | 2009 |
|
| Secondary structure models of the 3' untranslated regions of diverse R2 RNAs. | 2004-06 |
|
| Top-down characterization of nucleic acids modified by structural probes using high-resolution tandem mass spectrometry and automated data interpretation. | 2004-05-01 |
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3688-37-7
Created by
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107149
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2HAV7G194P
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222-986-3
Created by
admin on Mon Mar 31 20:30:37 GMT 2025 , Edited by admin on Mon Mar 31 20:30:37 GMT 2025
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DTXSID10863249
Created by
admin on Mon Mar 31 20:30:37 GMT 2025 , Edited by admin on Mon Mar 31 20:30:37 GMT 2025
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SUBSTANCE RECORD
