D136905
1,2-Dimethoxy-4-propenylbenzene
99%
Synonym(s):
Isoeugenyl methyl ether
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5 G
$53.20
About This Item
Linear Formula:
CH3CH=CHC6H3(OCH3)2
CAS Number:
Molecular Weight:
178.23
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
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description
mixture of isomers
Quality Level
assay
99%
form
liquid
refractive index
n20/D 1.568 (lit.)
bp
262-264 °C (lit.)
mp
98-100 °C (lit.)
density
1.05 g/mL at 25 °C (lit.)
SMILES string
COc1ccc(\C=C\C)cc1OC
InChI
1S/C11H14O2/c1-4-5-9-6-7-10(12-2)11(8-9)13-3/h4-8H,1-3H3/b5-4+
InChI key
NNWHUJCUHAELCL-SNAWJCMRSA-N
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Related Categories
Storage Class
10 - Combustible liquids
wgk_germany
WGK 2
flash_point_f
235.4 °F - closed cup
flash_point_c
113 °C - closed cup
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Alexander T Cartus et al.
Drug metabolism and disposition: the biological fate of chemicals, 39(9), 1727-1733 (2011-06-03)
Methylisoeugenol (1,2-dimethoxy-4-propenylbenzene, 1) is a minor constituent of essential oils, naturally occurring as a mixture of cis/trans isomers. 1 is a U.S. Food and Drug Administration-approved food additive and has been given "Generally Recognized as Safe" status. Previously, metabolism of
A call for full ingredient labelling and uniform nomenclature on medicaments.
A E Pink et al.
The British journal of dermatology, 161(2), 489-490 (2009-06-24)
Todd J Barkman
Molecular biology and evolution, 20(2), 168-172 (2003-02-25)
Isoeugenol-O-methyltransferase (IEMT) is an enzyme involved in the production of the floral volatile compounds methyl eugenol and methyl isoeugenol in Clarkia breweri (Onagraceae). IEMT likely evolved by gene duplication from caffeic acid-O-methyltransferase followed by amino acid divergence, leading to the
J Wang et al.
Plant physiology, 114(1), 213-221 (1997-05-01)
We have previously shown (R.A. Raguso, E. Pichersky [1995] Plant Syst Evol 194: 55-67) that the strong, sweet fragrance of Clarkia breweri (Onagraceae), an annual plant native to California, consists of 8 to 12 volatile compounds, including 4 phenylpropanoids. Although
Factors influencing conjugation of phenolic compounds with the epsilon-amino group.
Y Takeuchi
The Journal of dermatology, 12(2), 153-160 (1985-04-01)
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