Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C7H8O2 |
| Molecular Weight | 124.1372 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
COC1=CC(O)=CC=C1
InChI
InChIKey=ASHGTJPOSUFTGB-UHFFFAOYSA-N
InChI=1S/C7H8O2/c1-9-7-4-2-3-6(8)5-7/h2-5,8H,1H3
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Total synthesis of 10-norparvulenone and of O-methylasparvenone using a xanthate-mediated free radical addition-cyclization sequence. | 2003 Oct 2 |
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| An efficient and scalable synthesis of substituted phenanthrenequinones by intramolecular Friedel-Crafts reaction of imidazolides. | 2007 Oct 11 |
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| Thermochemistry and gas-phase ion energetics of 2-hydroxy-4-methoxy-benzophenone (oxybenzone). | 2008 Apr 10 |
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| Antioxidant hydroquinones substituted by beta-1,6-linked oligosaccharides in wheat germ. | 2009 Apr |
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| The bromination kinetics of phenolic compounds in aqueous solution. | 2009 Oct 30 |
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| Structure-toxicity relationship of phenolic analogs as anti-melanoma agents: an enzyme directed prodrug approach. | 2010 Feb 12 |
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| (E)-2-[(4-Fluoro-phen-yl)imino-meth-yl]-5-methoxy-phenol. | 2010 Jan 9 |
|
| Rate coefficients for the gas-phase reaction of hydroxyl radicals with 2-methoxyphenol (guaiacol) and related compounds. | 2010 Nov 4 |
Patents
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| Code System | Code | Type | Description | ||
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205-754-6
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DTXSID0022012
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150-19-6
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52678
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C094702
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9007
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HXB7441U87
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SUBSTANCE RECORD
