Carpacin

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Carpacin
Skeletal formula
Ball-and-stick model
Names
Preferred IUPAC name
5-Methoxy-6-[(E)-prop-1-enyl]-2H-1,3-benzodioxole[1]
Other names
(E)-5-Methoxy-6-(prop-1-en-1-yl)benzo[d][1,3]dioxole
(E)-2-Methoxy-4,5-methylenedioxypropenylbenzene
Identifiers
3D model (JSmol)
ChemSpider
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UNII
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  • InChI=1S/C11H12O3/c1-3-4-8-5-10-11(14-7-13-10)6-9(8)12-2/h3-6H,7H2,1-2H3/b4-3+ checkY
    Key: OTRFVHWXENKCEG-ONEGZZNKSA-N checkY
  • InChI=1/C11H12O3/c1-3-4-8-5-10-11(14-7-13-10)6-9(8)12-2/h3-6H,7H2,1-2H3/b4-3+
    Key: OTRFVHWXENKCEG-ONEGZZNKBF
  • C/C=C/C1=CC(OCO2)=C2C=C1OC
  • O1c2cc(c(OC)cc2OC1)/C=C/C
Properties
C11H12O3
Molar mass 192.214 g·mol−1
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).

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.[2]

Carpacin is a biosynthetic precursor of the more complex lignan-dimer, carpanone.[3] It is classified as a phenylpropanoid.

Carpacin has been prepared synthetically from sesamol[4] and has been studied for potential use as an insecticide[5] and inhibitor of carcinogenesis.[4]

References

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