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α-asarone

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EntityQ419658· pop 17· linked from 31 articles

α-asarone

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Also known as trans-Isoasarone, trans-Isoasaron, Asarone, trans-1,2,4-trimethoxy-5-(1-propenyl)benzene

Asarone is chemical compound of the phenylpropanoid class found in certain plants such as Acorus and Asarum. There are two isomers, α (or trans) and β (or cis). As a volatile fragrance oil, it is used in killing pests and bacteria.

In the Vinony graph

Within Vinony's link graph, α-asarone is referenced by 31 other articles, and connects out to International Standard Book Number, chemical compound and mass density.

It is catalogued under topics including Chembox image size set, Chemical articles with multiple CAS registry numbers and Chemical articles with multiple compound IDs.

Its subject is documented across 16 Wikipedia language editions.

Chemical data

Formula
C12H16O3
Molecular weight
208.25 g/mol
IUPAC name
1,2,4-trimethoxy-5-[(E)-prop-1-enyl]benzene
SMILES
C/C=C/C1=CC(=C(C=C1OC)OC)OC
InChIKey
RKFAZBXYICVSKP-AATRIKPKSA-N
XLogP
3
Polar surface area
27.7 Ų
H-bond donors
0
H-bond acceptors
3
Formal charge
0

via PubChem

Drug data · ChEMBL

Molecule type
Small molecule

via ChEMBL · EBI

Wikidata facts

Has part
carbon
Mass
208.11
Show 5 more facts
found in taxon
Asarum megacalyx
chemical formula
C₁₂H₁₆O₃
canonical SMILES
CC=CC1=CC(=C(C=C1OC)OC)OC
isomeric SMILES
C/C=C/C1=CC(=C(C=C1OC)OC)OC
Commons category
Asarone
Sources (2)

via Wikidata · CC0

~1 min read

Encyclopedic overview

3 sections
Contents
  • Pharmacology
  • See also
  • Notes and references

Asarone is chemical compound of the phenylpropanoid class found in certain plants such as Acorus and Asarum. There are two isomers, α (or trans) and β (or cis). As a volatile fragrance oil, it is used in killing pests and bacteria.

== Pharmacology == The main clinical symptom of asarone is prolonged vomiting that sometimes lasted more than 15 hours. Asarone is not metabolized to trimethoxyamphetamine as has been claimed by online vendors.

Excerpted from Wikipedia’s “α-asarone” article, available under the CC BY-SA 4.0 licence.

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