Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C5H4O2 |
| Molecular Weight | 96.0841 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
O=C1CC(=O)C=C1
InChI
InChIKey=MCFZBCCYOPSZLG-UHFFFAOYSA-N
InChI=1S/C5H4O2/c6-4-1-2-5(7)3-4/h1-2H,3H2
| Molecular Formula | C5H4O2 |
| Molecular Weight | 96.0841 |
| 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 |
|---|---|---|
| Cavity ringdown spectrum of the T(1)(n,pi*) <-- S(0) transition of 4-cyclopentene-1,3-dione. | 2009-11-26 |
|
| Experimental study on the thermal oxidation of 2-chlorophenol in air over the temperature range 450-900 degrees C. | 2006-03 |
|
| Design of hypoxia-targeting protein tyrosine kinase inhibitor using an innovative pharmacophore 2-methylene-4-cyclopentene-1,3-dione. | 2004-03-11 |
|
| Thermal decomposition of specifically phosphorylated D-glucoses and their role in the control of the Maillard reaction. | 2003-05-21 |
|
| Prostaglandin J2 metabolites inhibit aromatase activity by redox-sensitive mechanisms: potential implications for breast cancer therapy. | 2003-02-20 |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 19:02:52 GMT 2025
by
admin
on
Mon Mar 31 19:02:52 GMT 2025
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| Record UNII |
P054EQ880I
|
| Record Status |
Validated (UNII)
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| Record Version |
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