65420
4-Methoxycinnamic acid
≥98.0% (GC)
Synonym(s):
trans-3-(4-Methoxyphenyl)acrylic acid
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About This Item
Empirical Formula (Hill Notation):
C10H10O3
CAS Number:
Molecular Weight:
178.18
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
213-405-4
Beilstein/REAXYS Number:
2208397
MDL number:
Assay:
≥98.0% (GC)
InChI key
AFDXODALSZRGIH-QPJJXVBHSA-N
InChI
1S/C10H10O3/c1-13-9-5-2-8(3-6-9)4-7-10(11)12/h2-7H,1H3,(H,11,12)/b7-4+
SMILES string
COc1ccc(\C=C\C(O)=O)cc1
assay
≥98.0% (GC)
Storage Class
13 - Non 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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Yoshio Nakagawa et al.
Biochemical pharmacology, 66(1), 63-73 (2003-06-24)
The metabolism and action of trans-anethole (anethole) and the estrogen-like activity of the compound and its metabolites were studied in freshly isolated rat hepatocytes and cultured MCF-7 human breast cancer cells, respectively. The incubation of hepatocytes with anethole (0.25-2.0mM) caused
H V Meyers et al.
Carbohydrate research, 197, 15-32 (1990-03-25)
This study completes the spectroscopic basis for a novel oligosaccharide microanalytical method, wherein a derivatization sequence provides monosaccharide subunits bearing two types of exciton-coupling chromophore groups ("bichromophoric") for circular dichroic spectroscopy, namely 4-bromobenzoate (lambda max 245 nm) and 4-methoxycinnamate (lambda
Sirichai Adisakwattana et al.
International journal of molecular sciences, 13(2), 1778-1789 (2012-03-13)
Cinnamic acid and its derivatives have shown a variety of pharmacologic properties. However, little is known about the antiglycation properties of cinnamic acid and its derivatives. The present study sought to characterize the protein glycation inhibitory activity of cinnamic acid
Victor S Sobolev et al.
Journal of agricultural and food chemistry, 54(10), 3505-3511 (2006-05-17)
The peanut plant (Arachis hypogaea) is known to produce stilbene phytoalexins as a defensive response to fungal invasion; however, the distribution of phytoalexins among different organs of the peanut plant at early stages of growth under axenic conditions has not
N Ikemoto et al.
Carbohydrate research, 239, 11-33 (1993-02-01)
The microscale analytical method that is being developed in this group for the structure determination of oligosaccharides yields monosaccharide derivatives bearing two types of chromophores suitable for exciton-coupling, namely, 4-bromobenzoate (lambda max 245 nm) and 4-methoxycinnamate (lambda max 311 nm).
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