Home Other Building Blocks ethyl-(E)-cinnamate,ethyl-trans-cinnamate

ethyl-(E)-cinnamate,ethyl-trans-cinnamate

CAS No.:
4192-77-2
Catalog Number:
AG00CIXQ
Molecular Formula:
C11H12O2
Molecular Weight:
176.2118
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Product Description
Catalog Number:
AG00CIXQ
Chemical Name:
ethyl-(E)-cinnamate,ethyl-trans-cinnamate
CAS Number:
4192-77-2
Molecular Formula:
C11H12O2
Molecular Weight:
176.2118
MDL Number:
MFCD00009189
IUPAC Name:
ethyl (E)-3-phenylprop-2-enoate
InChI:
InChI=1S/C11H12O2/c1-2-13-11(12)9-8-10-6-4-3-5-7-10/h3-9H,2H2,1H3/b9-8+
InChI Key:
KBEBGUQPQBELIU-CMDGGOBGSA-N
SMILES:
CCOC(=O)C=Cc1ccccc1
EC Number:
203-104-6
UNII:
C023P3M5JJ
NSC Number:
6773
FEMA Number:
2430
Properties
Complexity:
179  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
1  
Exact Mass:
176.084g/mol
Formal Charge:
0
Heavy Atom Count:
13  
Hydrogen Bond Acceptor Count:
2  
Hydrogen Bond Donor Count:
0
Isotope Atom Count:
0
Molecular Weight:
176.215g/mol
Monoisotopic Mass:
176.084g/mol
Rotatable Bond Count:
4  
Topological Polar Surface Area:
26.3A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
3  
Literature
Title Journal
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Radical scavenging activity of lipophilized products from lipase-catalyzed transesterification of triolein with cinnamic and ferulic acids. Lipids 20090201
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A concise, asymmetric synthesis of (2R,3R)-3-hydroxyaspartic acid. Amino acids 20080801
Larvicidal activity of Kaempferia galanga rhizome phenylpropanoids towards three mosquito species. Pest management science 20080801
Fragrance material review on ethyl cinnamate. Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association 20070101
Prediction of estrogen receptor agonists and characterization of associated molecular descriptors by statistical learning methods. Journal of molecular graphics & modelling 20061101
Sun protection enhancement of titanium dioxide crystals by the use of carnauba wax nanoparticles: the synergistic interaction between organic and inorganic sunscreens at nanoscale. International journal of pharmaceutics 20060928
[Estrogenic activity of ultraviolet absorbers and the related compounds]. Yakugaku zasshi : Journal of the Pharmaceutical Society of Japan 20050801
Esters, amides and substituted derivatives of cinnamic acid: synthesis, antimicrobial activity and QSAR investigations. European journal of medicinal chemistry 20041001
Structure-activity relationships of trans-cinnamic acid derivatives on alpha-glucosidase inhibition. Bioorganic & medicinal chemistry letters 20040607
Vasorelaxant effects of ethyl cinnamate isolated from Kaempferia galanga on smooth muscles of the rat aorta. Planta medica 20020701
Pine weevil (Hylobius abietis) antifeedants from lodgepole pine (Pinus contorta). Journal of chemical ecology 20011101
Structure-activity relationships for a large diverse set of natural, synthetic, and environmental estrogens. Chemical research in toxicology 20010301
Properties