320617
Ethyl 4-hydroxy-3-methoxycinnamate
98%
Synonyme(s) :
Ethyl ferulate
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A propos de cet article
Formule linéaire :
HOC6H3(OCH3)CH=CHCO2C2H5
Numéro CAS:
Poids moléculaire :
222.24
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
223-745-5
MDL number:
Assay:
98%
Form:
solid
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98%
form
solid
bp
164-166 °C/0.5 mmHg (lit.)
mp
63-65 °C (lit.)
functional group
ester
SMILES string
CCOC(=O)\C=C\c1ccc(O)c(OC)c1
InChI
1S/C12H14O4/c1-3-16-12(14)7-5-9-4-6-10(13)11(8-9)15-2/h4-8,13H,3H2,1-2H3/b7-5+
InChI key
ATJVZXXHKSYELS-FNORWQNLSA-N
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Classe de stockage
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
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Yan Zheng et al.
Bioresource technology, 100(12), 2896-2901 (2009-03-04)
Feruloylated diacylglycerol (FDAG) was synthesized using a selective lipase-catalyzed the transesterification between ethyl ferulate and triolein. To optimize the reaction conversion and purity of FDAG, dual response surface was applied to determine the effects of five-level-five-factors and their reciprocal interactions
Mirko Bunzel et al.
Journal of agricultural and food chemistry, 56(21), 10368-10375 (2008-10-10)
Valuable information about possible types of linkages, reaction mechanisms, and sequences for oxidative coupling of phenolic compounds in planta is available from in vitro model systems. Ferulate oligomers were generated in a system using ethyl ferulate, peroxidase, and hydrogen peroxide
Yun Feng et al.
Biochimica et biophysica acta, 1780(4), 659-672 (2008-01-31)
It is an important therapeutic strategy to protect mitochondria from oxidative stress, especially during ischemia-reperfusion. In the present study, an attempt has been made to evaluate the protective effects of caffeic acid phenethyl ester (CAPE) and its related phenolic compounds