320617

Ethyl 4-hydroxy-3-methoxycinnamate

Name: Ethyl 4-hydroxy-3-methoxycinnamate
Brand: ALDRICH

98%

Sinónimos:

Ethyl ferulate

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About This Item

Fórmula lineal:

HOC₆H₃(OCH₃)CH=CHCO₂C₂H₅

Número CAS:

4046-02-0

Peso molecular:

222.24

NACRES:

NA.22

PubChem Substance ID:

24859274

UNSPSC Code:

12352100

EC Number:

223-745-5

MDL number:

MFCD00009190

Nombre del producto

Ethyl 4-hydroxy-3-methoxycinnamate, 98%

InChI key

ATJVZXXHKSYELS-FNORWQNLSA-N

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+

SMILES string

CCOC(=O)\C=C\c1ccc(O)c(OC)c1

assay

98%

form

solid

bp

164-166 °C/0.5 mmHg (lit.)

mp

63-65 °C (lit.)

functional group

ester

signalword

Warning

hcodes

H315,H319,H335

pcodes

P261 - P264 - P271 - P280 - P302 + P352 - P305 + P351 + P338

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Clase de almacenamiento

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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In vivo protection of synaptosomes by ferulic acid ethyl ester (FAEE) from oxidative stress mediated by 2,2-azobis(2-amidino-propane)dihydrochloride (AAPH) or Fe(2+)/H(2)O(2): insight into mechanisms of neuroprotection and relevance to oxidative stress-related neurodegenerative disorders.

Gururaj Joshi et al.

Neurochemistry international, 48(4), 318-327 (2006-01-03)

Ferulic acid ethyl ester (FAEE) is an ester derivative of ferulic acid, the latter known for its anti-inflammatory and antioxidant properties. Previous studies from our laboratory have shown that ferulic acid protects synaptosomal membrane system and neuronal cell culture systems

Dual response surface-optimized process for feruloylated diacylglycerols by selective lipase-catalyzed transesterification in solvent free system.

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

Detection of ferulic acid esterase production by Bacillus spp. and lactobacilli.

J Donaghy et al.

Applied microbiology and biotechnology, 50(2), 257-260 (1998-10-09)

The production of feruloyl esterase activity by Bacillus spp. and lactobacilli can be detected in an agarplate assay. The assay involves the substitution of the main carbon source in specific agar with ethyl ferulate. A number of Bacillus spp., predominantly

Peroxidase-catalyzed oligomerization of ferulic acid esters.

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

Screening and analysis of an antineoplastic compound in Rhizoma Chuanxiong by means of in vitro metabolism and HPLC-MS.

Liang Kong et al.

Analytical and bioanalytical chemistry, 386(2), 264-274 (2006-07-27)

A new screening and analysis method that combines in vitro metabolism with high-performance liquid chromatography-mass spectrometry (HPLC-MS) was developed for the screening and analysis of an antineoplastic compound, coniferyl ferulate, which is present in the rhizome of Rhizoma Chuanxiong. Infrared

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