Weight | 147.177 g/mol |
---|---|
Formula | C9H9NO |
Hydrogen Acceptors | 1 |
Hydrogen Donors | 1 |
Aromatic Rings | 1 |
Rotatable Bonds | 2 |
CINNAMAMIDE (621-79-4, 22031-64-7)
Score:
#29 in Medicinal chemistry
,
#5835 in Chemistry
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- In situ X-ray observation of pedal-like conformational change and dimerization of trans-cinnamamide in cocrystals with phthalic acid. (Journal of the American Chemical Society, 2001)
- Synthesis, Properties, and Light-Induced Shape Memory Effect of Multiblock Polyesterurethanes Containing Biodegradable Segments and Pendant Cinnamamide Groups (Biomacromolecules, 2011)
- Cinnamamide analogs as inhibitors of protein tyrosine kinases. (Farmaco, 1993)
- Absolute asymmetric photochemistry using centrosymmetric single crystals. The host/guest system (E)-cinnamamide/E-cinnamic acid (Journal of the American Chemical Society, 1989)
- Biosynthesis of cinnamamide and detection of phenylalanine ammonia-lyase in Streptomyces verticillatus (Canadian Journal of Microbiology, 1970)
- Cinnamamide derivatives from Clausena lansium (Phytochemistry, 1989)
-
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1=CC=C(C=C1)C=CC(=O)N
-
InChIKeyAPEJMQOBVMLION-UHFFFAOYSA-N
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Synthesis
Reactant
+
CHLOROBENZENE
(Stille)
Reactant
+
1-Hydroxy-1,2-benziodoxol-3(1H)-one 1-oxide
(Nicolaou IBX dehydrogenation)
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