| Stereochemistry | ACHIRAL |
| Molecular Formula | C7H8O3 |
| Molecular Weight | 140.1366 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
OCC1=CC(O)=CC=C1O
InChI
InChIKey=PUZSUVGRVHEUQO-UHFFFAOYSA-N
InChI=1S/C7H8O3/c8-4-5-3-6(9)1-2-7(5)10/h1-3,8-10H,4H2
| Molecular Formula | C7H8O3 |
| Molecular Weight | 140.1366 |
| Charge | 0 |
| Count |
MOL RATIO
1 MOL RATIO (average) |
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Parasitenone, a new epoxycyclohexenone related to gabosine from the marine-derived fungus Aspergillus parasiticus. | 2002 May |
|
| Screening for metabolites from Penicillium novae-zeelandiae displaying radical-scavenging activity and oxidative mutagenicity: isolation of gentisyl alcohol. | 2003 Aug 5 |
|
| Gentisyl alcohol derivatives from the marine-derived fungus Penicillium terrestre. | 2008 Jan |
|
| Molecular cloning and functional characterization of two CYP619 cytochrome P450s involved in biosynthesis of patulin in Aspergillus clavatus. | 2009 May |
|
| Biosynthesis and toxicological effects of patulin. | 2010 Apr |
|
| Dual reactivity of hydroxy- and methoxy- substituted o-quinone methides in aqueous solutions: hydration versus tautomerization. | 2010 Nov 5 |
Patents
| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
|
m743 | PRIMARY | Merck Index | ||
|
495-08-9 | PRIMARY | |||
|
T8T2WY38GH | PRIMARY | |||
|
188287 | PRIMARY | |||
|
5325 | PRIMARY | |||
|
DTXSID60197804 | PRIMARY |