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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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.
Life sciences, 78(4), 406-412 (2005-09-06)
We investigated the antihyperglycemic effect of p-methoxycinnamic acid (p-MCA), a cinnamic acid derivative, on plasma glucose and insulin concentrations, activities of hepatic glucose-regulating enzymes and hepatic glycogen content in normal and streptozotocin (STZ)-induced diabetic rats. p-MCA (10-100 mg/kg, PO) dose-dependently
So Ra Kim et al.
British journal of pharmacology, 135(5), 1281-1291 (2002-03-06)
1. We previously reported that four new phenylpropanoid glycosides and six known cinnamate derivatives isolated from roots of Scrophularia buergeriana Miquel (Scrophulariaceae) protected cultured cortical neurons from neurotoxicity induced by glutamate. Here, we have investigated the structure-activity relationships in the
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
H M Chawla et al.
Journal of photochemistry and photobiology. B, Biology, 105(1), 25-33 (2011-08-02)
A series of novel calix[4]arene enones (5-7) and cinnamates (12-14) have been synthesized and evaluated for ensuring protection from ultraviolet radiation (UVR). Spectroscopic analyses has revealed that compound 6 absorbs ultraviolet radiations between 280 and 350 nm with an absorption
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