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Carpacin

Structure via PubChem · Public domain (PubChem)

EntityQ5045595· pop 8· linked from 19 articles

Carpacin is a naturally occurring organic compound first isolated from the Carpano tree (an unidentified Cinnamomum species of the family Lauraceae which is native to Bougainville Island), from which it derives its name. It is also found in essential oils of the genus Crowea.

Chemical data

Formula
C11H12O3
Molecular weight
192.21 g/mol
IUPAC name
5-methoxy-6-[(E)-prop-1-enyl]-1,3-benzodioxole
SMILES
C/C=C/C1=CC2=C(C=C1OC)OCO2
InChIKey
OTRFVHWXENKCEG-ONEGZZNKSA-N
XLogP
2.7
Polar surface area
27.7 Ų
H-bond donors
0
H-bond acceptors
3
Formal charge
0

via PubChem

Wikidata facts

Mass
192.078644
Show 4 more facts
Commons category
Carpacin
chemical formula
C₁₁H₁₂O₃
isomeric SMILES
C/C=C/C1=CC2=C(C=C1OC)OCO2
canonical SMILES
CC=CC1=CC2=C(C=C1OC)OCO2
Sources (1)

via Wikidata · CC0

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Encyclopedic overview

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Contents
  • References

Carpacin is a naturally occurring organic compound first isolated from the Carpano tree (an unidentified Cinnamomum species of the family Lauraceae which is native to Bougainville Island), from which it derives its name. It is also found in essential oils of the genus Crowea.

Carpacin is a biosynthetic precursor of the more complex lignan-dimer, carpanone. It is classified as a phenylpropanoid.

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

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