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D136905

Sigma-Aldrich

1,2-Dimethoxy-4-propenylbenzene

99%

Synonym(s):

Isoeugenyl methyl ether

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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

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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Storage Class Code

10 - Combustible liquids

WGK

WGK 2

Flash Point(F)

235.4 °F - closed cup

Flash Point(C)

113 °C - closed cup


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T Jia et al.
Zhongguo Zhong yao za zhi = Zhongguo zhongyao zazhi = China journal of Chinese materia medica, 22(8), 474-475 (1997-08-01)
A HPLC method for the determination of eugenol, methyleugenol and methylisoeugenol in the volatile oil of differently processed natmeg has been used. The result has shown that the content of eugenol is only sliahtly changed before and after processing, but
Jeong-Yeh Yang et al.
The Journal of nutritional biochemistry, 20(7), 537-543 (2008-09-16)
We report here that octanoate and decanoate, 8-carbon and 10-carbon medium-chain fatty acids (MCFA), decreased adipogenesis in 3T3-L1 preadipocytes when treated with standard hormonal cocktail, but increased adipogenesis in a dose-dependent manner (with decanoate being more effective) when treated with
Influence of vehicles on penetration through human epidermis of benzyl alcohol, isoeugenol and methyl isoeugenol.
Y Jimbo et al.
The Journal of dermatology, 10(3), 241-250 (1983-06-01)
Factors influencing conjugation of phenolic compounds with the epsilon-amino group.
Y Takeuchi
The Journal of dermatology, 12(2), 153-160 (1985-04-01)
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

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