Ethyl ferulate
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Ethyl ferulate
structure -
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CAS No:
4046-02-0
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Formula:
C12H14O4
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Chemical Name:
Ethyl ferulate
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Synonyms:
2-Propenoic acid,3-(4-hydroxy-3-methoxyphenyl)-,ethyl ester;Cinnamic acid,4-hydroxy-3-methoxy-,ethyl ester;Ferulic acid ethyl ester;Ethyl ferulate;Ethyl 4-hydroxy-3-methoxycinnamate;BBR 3222;NSC 14879;Ethyl 3-(4-hydroxy-3-methoxyphenyl)acrylate
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CAS No:
Description
Ethyl ferulate, a naturally lipophilic derivative of ferulic acid originally derived from giant fennel (F. communis), induces heme oxygenase-1 (HO-1) and protects rat neurons against oxidative stress[1]. Ethyl ferulate also protects neurons against amyloid β peptide (1-42)-induced oxidative stress and neurotoxicity[2].
Characteristics
55.8
2.2
1.2±0.1 g/cm3
75.5-76.5 °C
164-166 °C @ Press: 0.5 Torr
132.5±17.2 °C
1.566
2.17E-06mmHg at 25°C
Safety Information
NONH for all modes of transport
3
36/37/38
26-37/39-36
Xi
Irritant
P261-P305 + P351 + P338
H315-H319-H335
|Warning|H315 (100%): Causes skin irritation [Warning Skin corrosion/irritation]|P261, P264, P271, P280, P302+P352, P304+P340, P305+P351+P338, P312, P321, P332+P313, P337+P313, P362, P403+P233, P405, and P501|Aggregated GHS information provided by 40 companies from 3 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.
Ethyl ferulate Use and Manufacturing
It is the basic raw material for the production of drugs for the treatment of cardiovascular and cerebrovascular diseases and leukopenia.
Computed Properties
Molecular Weight:222.24
XLogP3:2.2
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:5
Exact Mass:222.08920892
Monoisotopic Mass:222.08920892
Topological Polar Surface Area:55.8
Heavy Atom Count:16
Complexity:249
Defined Bond Stereocenter Count:1
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes
Drug Function and Efficacy
Antioxidant and UV-protective compound; stabilizes formulations and protects skin from photo-damage.
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