146242
3,4-(Methylenedioxy)cinnamic acid, predominantly trans
99%
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About This Item
Empirical Formula (Hill Notation):
C10H8O4
CAS Number:
Molecular Weight:
192.17
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
219-151-0
MDL number:
Assay:
99%
Form:
powder
Product Name
3,4-(Methylenedioxy)cinnamic acid, predominantly trans, 99%
InChI key
QFQYZMGOKIROEC-DUXPYHPUSA-N
InChI
1S/C10H8O4/c11-10(12)4-2-7-1-3-8-9(5-7)14-6-13-8/h1-5H,6H2,(H,11,12)/b4-2+
SMILES string
OC(=O)\C=C\c1ccc2OCOc2c1
assay
99%
form
powder
mp
242-244 °C (dec.) (lit.)
functional group
carboxylic acid
Quality Level
Related Categories
General description
3,4-(Methylenedioxy)cinnamic acid is an inhibitor of the phenylpropanoid enzyme 4-hydroxycinnamoyl-CoA ligase. It undergoes electron transfer reaction with trichloromethylperoxyl radical and reaction has been studied by pulse radiolysis.
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
Regulatory Information
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Rogério Barbosa Lima et al.
PloS one, 8(12), e80542-e80542 (2013-12-07)
Cinnamic acid and its hydroxylated derivatives (p-coumaric, caffeic, ferulic and sinapic acids) are known allelochemicals that affect the seed germination and root growth of many plant species. Recent studies have indicated that the reduction of root growth by these allelochemicals
J X Pan et al.
Free radical research, 30(3), 241-245 (2000-03-11)
The electron transfer reactions between the trichloromethylperoxyl radical (Cl3COO*) and hydroxycinnamic acid derivatives, including chlorogenic acid, sinapic acid, caffeic acid, ferulic acid and 3,4-(methylenedioxy)cinnamic acid, have been studied by pulse radiolysis. The hydroxycinnamic acid derivatives, especially sinapic acid, are identified
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