Names | |
---|---|
Preferred IUPAC name
4,5-Dimethoxy-6-(prop-2-en-1-yl)-2H-1,3-benzodioxole | |
Other names
6-Allyl-4,5-dimethoxybenzo[d][1,3]dioxole
1-Allyl-2,3-dimethoxy-4,5-(methylenedioxy)benzene | |
Identifiers | |
3D model (
JSmol)
|
|
ChEMBL | |
ChemSpider | |
ECHA InfoCard | 100.149.911 |
EC Number |
|
KEGG | |
PubChem
CID
|
|
UNII | |
| |
| |
Properties | |
C12H14O4 | |
Molar mass | 222.240 g·mol−1 |
Density | 1.163 g/cm3 |
Except where otherwise noted, data are given for materials in their
standard state (at 25 °C [77 °F], 100 kPa).
|
Dillapiole is an organic chemical compound and essential oil commonly extracted from dill weed, though it can be found in a variety of other plants such as fennel root. [1] This compound is closely related to apiole, having a methoxy group positioned differently on the benzene ring. [2] [3] Dillapiole works synergically with certain insecticides like pyrethrins similarly to piperonyl butoxide, which likely results from inhibition of the MFO enzyme of insects. [4]
No carcinogenicity was detected with parsley apiol or dill apiol in mice. [5]
Names | |
---|---|
Preferred IUPAC name
4,5-Dimethoxy-6-(prop-2-en-1-yl)-2H-1,3-benzodioxole | |
Other names
6-Allyl-4,5-dimethoxybenzo[d][1,3]dioxole
1-Allyl-2,3-dimethoxy-4,5-(methylenedioxy)benzene | |
Identifiers | |
3D model (
JSmol)
|
|
ChEMBL | |
ChemSpider | |
ECHA InfoCard | 100.149.911 |
EC Number |
|
KEGG | |
PubChem
CID
|
|
UNII | |
| |
| |
Properties | |
C12H14O4 | |
Molar mass | 222.240 g·mol−1 |
Density | 1.163 g/cm3 |
Except where otherwise noted, data are given for materials in their
standard state (at 25 °C [77 °F], 100 kPa).
|
Dillapiole is an organic chemical compound and essential oil commonly extracted from dill weed, though it can be found in a variety of other plants such as fennel root. [1] This compound is closely related to apiole, having a methoxy group positioned differently on the benzene ring. [2] [3] Dillapiole works synergically with certain insecticides like pyrethrins similarly to piperonyl butoxide, which likely results from inhibition of the MFO enzyme of insects. [4]
No carcinogenicity was detected with parsley apiol or dill apiol in mice. [5]