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T70408

3,4,5-Trimethoxycinnamic acid

97%

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About This Item

Linear Formula:
(CH3O)3C6H2CH=CHCO2H
CAS Number:
90-50-6
Molecular Weight:
238.24
UNSPSC Code:
12352100
PubChem Substance ID:
24900246
EC Number:
201-999-8
MDL number:
MFCD00004388
Assay:
97%
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assay

97%

mp

125-127 °C (lit.)

SMILES string

COc1cc(\C=C\C(O)=O)cc(OC)c1OC

InChI

1S/C12H14O5/c1-15-9-6-8(4-5-11(13)14)7-10(16-2)12(9)17-3/h4-7H,1-3H3,(H,13,14)/b5-4+

InChI key

YTFVRYKNXDADBI-SNAWJCMRSA-N

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pictograms

Exclamation mark
GHS07

signalword

Warning

hcodes

H317,H319

Hazard Classifications

Eye Irrit. 2 - Skin Sens. 1

Storage Class

11 - Combustible Solids

wgk

WGK 2

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

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Certificates of Analysis (COA)

Lot/Batch Number
BCCC8678
1404102V
1402646V
07204EV
1404102

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[The detection of Azotobacter and its significance in criminal technical soil examinations].
E Kissling
Archiv fur Kriminologie, 165(1-2), 27-34 (1980-01-01)
Sarvesh Kumar et al.
Biochemistry, 44(48), 15944-15952 (2005-11-30)
We report here the isolation and characterization of two active principles, ethyl 3',4',5'-trimethoxycinnamate (1) and piperine (2), from the combined hexane and chloroform extracts of Piper longum. Using primary human umbilical vein endothelial cells, we evaluated the activities of compound
Jae-Chul Jung et al.
Chemical biology & drug design, 81(3), 389-398 (2012-11-06)
A series of 3,4,5-trimethoxycinnamic acid derivatives was prepared and evaluated for antinarcotic effects on morphine dependence in mice and binding affinities on serotonergic receptors. The key synthetic strategies involve generation of ketones 6-7, esters 9-12 through condensation reaction, and amides
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Global Trade Item Number

SKUGTIN
T70408-25G04061837372278