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You are currently exploring Chavibetol.
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Two skeleton analogues:
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Analogue 1: With cis-Phenylprop-1-ene skeleton
cis-3-Hydroxy-4-methoxyphenylprop-1-ene Formula: C10H12O2. PubChem ID: 1781947. ChemSpider ID: 1401086. Essential oil. |
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Analogue 2: With trans-Phenylprop-1-ene skeleton
trans-3-Hydroxy-4-methoxyphenylprop-1-ene Formula: C10H12O2. PubChem ID: 1789147. ChemSpider ID: 1401088. Essential oil. |
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Two R3 analogues:
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Analogue 1: Removing Hydroxy at R3
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Analogue 2: Substituting Methoxy for Hydroxy at R3
Methyleugenol; 3,4-Dimethoxyphenylprop-2-ene Formula: C11H14O2. PubChem ID: 7127. ChemSpider ID: 21106140. Wikipedia: Eugenol. Essential oil.
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Five isomers:
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Isomer 1
Eugenol; 4-Hydroxy-3-methoxyphenylprop-2-ene Formula: C10H12O2. PubChem ID: 3314. ChemSpider ID: 13876103. Wikipedia: Eugenol. Essential oil.
Shulgin, AT. Composition of the myristicin fraction from oil of nutmeg. Nature, 1963, 197, 379. |
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Isomer 2
cis-4-Hydroxy-3-methoxyphenylprop-1-ene Formula: C10H12O2. PubChem ID: 1549041. ChemSpider ID: 1266028. Essential oil. |
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Isomer 3
Isoeugenol; trans-4-Hydroxy-3-methoxyphenylprop-1-ene Formula: C10H12O2. PubChem ID: 853433. ChemSpider ID: 21106129. Essential oil.
Shulgin, AT. Composition of the myristicin fraction from oil of nutmeg. Nature, 1963, 197, 379. |
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Isomer 4
cis-3-Hydroxy-4-methoxyphenylprop-1-ene Formula: C10H12O2. PubChem ID: 1781947. ChemSpider ID: 1401086. Essential oil. |
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Isomer 5
trans-3-Hydroxy-4-methoxyphenylprop-1-ene Formula: C10H12O2. PubChem ID: 1789147. ChemSpider ID: 1401088. Essential oil. |
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