528420
4-Ethoxycinnamic acid, predominantly trans
97%
Sign In to View Organizational & Contract Pricing.
Select a Size
About This Item
Linear Formula:
C2H5OC6H4CH=CHCO2H
CAS Number:
Molecular Weight:
192.21
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
MDL number:
Assay:
97%
InChI
1S/C11H12O3/c1-2-14-10-6-3-9(4-7-10)5-8-11(12)13/h3-8H,2H2,1H3,(H,12,13)/b8-5+
SMILES string
CCOc1ccc(\C=C\C(O)=O)cc1
InChI key
DZLOUWYGNATKKZ-VMPITWQZSA-N
assay
97%
mp
195-199 °C (lit.)
General description
4-Ethoxycinnamic acid can be synthesized by reacting the corresponding aryl aldehyde with malonic acid. It participates in the synthesis of cholest-5-en-3βyl 3-(4-ethoxyphenyl)-prop-2-enoate.
Storage Class
13 - Non Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
Regulatory Information
新产品
This item has
Choose from one of the most recent versions:
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
Cholest-5-en-3?-yl 3-(4-ethoxyphenyl) prop-2-enoate.
Bugenhagen B, et al.
Acta Crystallographica Section E, Structure Reports Online, 68(7), o2064-o2064 (2012)
T R Herrin et al.
Journal of medicinal chemistry, 18(12), 1216-1223 (1975-12-01)
The preparation and activity against Plasmodium berghei of derivatives of 1-(4-methoxycinnamoyl)-4-(5-phenyl-4-oxo-2-oxazolin-2-yl)piperazine are described. Replacement of the cinnamoyl group was accomplished by acylation or alkylation of 1-(5-phenyl-4-oxo-2-oxazolin-2-yl)piperazine. Modifications of the 5-phenyl group were prepared either by a sequence of reactions involving
Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.
Contact Technical Service