22329-76-6

22329-76-6 structure

Name: Methyl ferulate
Chemical Name: ethyl 4-hydroxy-3-methoxycinnamate
CAS Number: 22329-76-6
Molecular Formula: C₁₁H₁₂O₄
Molecular Weight: 208.211
Catalog: Natural product Phenylpropanoid
Create Date: 2018-10-08 18:50:19
Modify Date: 2024-01-01 20:29:07
(E)-Ferulic acid methyl ester (Methyl (E)-ferulate) exhibits strong DPPH and ABTS+ radical scavenging activities[1].

Name	ethyl 4-hydroxy-3-methoxycinnamate
Synonyms	Ferulic acid methyl ester Methyl (2E)-3-(4-hydroxy-3-methoxyphenyl)acrylate 3,7,11-trimethyl-dodeca-2,6,10-trienoic acid methyl ester Methyl-3,7,11-trimethyldodeca-2,6,10-trienoat MFCD00017208 2-Propenoic acid, 3- (4-hydroxy-3-methoxyphenyl)-, methyl ester methyl 3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate 2-Propenoic acid, 3-(4-hydroxy-3-methoxyphenyl)-, methyl ester, (2E)- methyl farnesoate methyl ester of 4-hydroxy-3-methoxycinnamic acid 2-Propenoic acid, 3-(4-hydroxy-3-methoxyphenyl)-, methyl ester (9CI) Methyl ferulate methyl farneosate methyl farnesate Farnesyl methyl ester Methyl 4-hydroxy-3-methoxycinnamate EINECS 225-747-1 3,7,11-Trimethyl-dodeca-2,6,10-triensaeure-methylester 2,6,10-Dodecatrienoic acid,3,7,11-trimethyl-,methyl ester trans-Ferulic acid methyl ester

Description	(E)-Ferulic acid methyl ester (Methyl (E)-ferulate) exhibits strong DPPH and ABTS+ radical scavenging activities[1].
Related Catalog	Research Areas >> Others Signaling Pathways >> Others >> Others
References	[1]. Wei Wang, et al.Isolation, identification and antioxidant activity of bound phenolic compounds present in rice bran. Food Chem. 2015 Mar 15;171:40-9.

Density	1.2±0.1 g/cm3
Boiling Point	338.1±27.0 °C at 760 mmHg
Melting Point	63-65ºC(lit.)
Molecular Formula	C₁₁H₁₂O₄
Molecular Weight	208.211
Flash Point	130.4±17.2 °C
Exact Mass	208.073563
PSA	55.76000
LogP	1.40
Vapour Pressure	0.0±0.8 mmHg at 25°C
Index of Refraction	1.575
Storage condition	2-8℃
Water Solubility	Slightly soluble (2.3 g/L) (25 ºC)

Hazard Codes	Xi: Irritant;
Risk Phrases	R36/37/38
Safety Phrases	26-37/39
WGK Germany	3

67-56-1

1135-24-6

~88%

22329-76-6

Literature: Junek, Richard; Kverka, Miloslav; Jandera, Antonin; Panajotova, Vladimira; Satinsky, Dalibor; Machacek, Milos; Kuchar, Miroslav European Journal of Medicinal Chemistry, 2009 , vol. 44, # 1 p. 332 - 344

1135-24-6

~86%

22329-76-6

Literature: Figlus, Marek; Tarruella, Albert C.; Messer, Anastasia; Sollis, Steven L.; Hartley, Richard C. Chemical Communications, 2010 , vol. 46, # 24 p. 4405 - 4407

1135-24-6

149-73-5

~99%

22329-76-6

Literature: Comi, Marc; Lligadas, Gerard; Ronda, Juan C.; Galia, Marina; Cadiz, Virginia Journal of Polymer Science, Part A: Polymer Chemistry, 2013 , vol. 51, # 22 p. 4894 - 4903

16695-14-0

121-33-5

~77%

22329-76-6

Literature: Wang, Huan; Wei, Qing-Yi; Jiang, Hong; Jiang, Zhen-Hua Research on Chemical Intermediates, 2012 , vol. 38, # 1 p. 207 - 213

107647-22-3

22329-76-6

Literature: Nakano; Murakami; Takaishi; Tomimatsu Chemical and Pharmaceutical Bulletin, 1986 , vol. 34, # 12 p. 5005 - 5010

1445-45-0

1135-24-6

~10%

22329-76-6

Literature: Lee, Jong Chan; Song, In-Goul; Park, Jin Young Synthetic Communications, 2002 , vol. 32, # 14 p. 2209 - 2213

121-33-5

22329-76-6

Literature: Gustafsson, Mikaela; Kaerkoenen, Anna; Simola, Liisa K; Teeri, Teemu H; Sipilae, Jussi; Kilpelaeinen, Ilkka; Brunow, Goesta Phytochemistry, 2001 , vol. 58, # 2 p. 243 - 248

Precursor 7
67-56-1 1135-24-6 149-73-5 16695-14-0
121-33-5 107647-22-3 1445-45-0
DownStream 2
3843-74-1 214779-01-8

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