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65400

Sigma-Aldrich

2-Methoxycinnamic acid

≥97.0%

Synonym(s):

3-(2-Methoxyphenyl)acrylic acid

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About This Item

Empirical Formula (Hill Notation):
C10H10O3
CAS Number:
6099-03-2
Molecular Weight:
178.18
Beilstein/REAXYS Number:
2209714
EC Number:
228-047-4
MDL number:
MFCD00064238
UNSPSC Code:
12352100
PubChem Substance ID:
57652029
NACRES:
NA.22

assay

≥97.0%

mp

182-186 °C

functional group

carboxylic acid

SMILES string

COc1ccccc1\C=C\C(O)=O

InChI

1S/C10H10O3/c1-13-9-5-3-2-4-8(9)6-7-10(11)12/h2-7H,1H3,(H,11,12)/b7-6+

InChI key

FEGVSPGUHMGGBO-VOTSOKGWSA-N

pictograms

Exclamation mark
GHS07

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
STBF4082V

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Ninghui Ma et al.
Molecules (Basel, Switzerland), 23(9) (2018-09-12)
To rapidly clarify and quantify the chemical profiling of Cinnamomi cortex a reliable and feasible strategy of chromatographic fingerprinting with a suite of chemometrics methods was developed and validated by ultra-high performance liquid chromatography coupled with diode array detection. Furthermore
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

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