320617
4-羟基-3-甲氧基肉桂酸乙酯
98%
别名:
阿魏酸乙酯
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关于此项目
线性分子式:
HOC6H3(OCH3)CH=CHCO2C2H5
化学文摘社编号:
分子量:
222.24
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
223-745-5
MDL number:
Assay:
98%
Form:
solid
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
Quality Level
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
K J Rashamuse et al.
Journal of applied microbiology, 103(5), 1610-1620 (2007-10-24)
Isolation and identification of bacterial isolates with specific ferulic acid (FA) esterase activity and cloning of a gene encoding activity. A micro-organism with ethyl ferulate hydrolysing (EFH) activity was isolated by culture enrichment techniques. Detailed molecular identification based on species-specific
T Nakayama et al.
Bioscience, biotechnology, and biochemistry, 60(2), 316-318 (1996-02-01)
Cytotoxicity and DNA single-strand breaks caused by H2O2 were assessed by a colony formation assay and a DNA precipitation assay, respectively, with Chinese hamster V79 cells. In both assays, caffeic acid ethyl ester showed protective effects. The structure-activity relationship showed
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
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
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
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