Weight | 180.25 g/mol |
---|---|
Formula | C14H12 |
Hydrogen Acceptors | 0 |
Hydrogen Donors | 0 |
Aromatic Rings | 2 |
Rotatable Bonds | 2 |
trans-Stilbene (103-30-0, 588-59-0)
Score:
#1014 in Physics
,
#2891 in Chemistry
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- Hereditary differences in the expression of the human glutathione transferase active on trans-stilbene oxide are due to a gene deletion (Proceedings of the National Academy of Sciences of the United States of America, 1988)
- Ultraviolet Spectra of Stilbene, pMonohalogen Stilbenes, and Azobenzene and the trans to cis Photoisomerization Process (Journal of Chemical Physics, 1962)
- Conformational Information from Vibrational Spectra of Styrene, trans-Stilbene, and cis-Stilbene (Journal of Physical Chemistry A, 1997)
- Piceatannol (3,4,3,5-tetrahydroxy-trans-stilbene) is a naturally occurring protein-tyrosine kinase inhibitor (Biochemical and Biophysical Research Communications, 1989)
- Ab initio study of cis-trans photoisomerization in stilbene and ethylene (Journal of Physical Chemistry A, 2003)
- Calculation of vibronic structure of the * transition of trans and cisstilbene (Journal of Chemical Physics, 1975)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1=CC=C(C=C1)C=CC2=CC=CC=C2
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InChIKeyPJANXHGTPQOBST-UHFFFAOYSA-N
- Pubchem - trans-Stilbene
- Wikipedia - (E)-stilbene
(E)-Stilbene, commonly known as trans-stilbene, is an organic compound represented by the condensed structural formula C6H5CH=CHC6H5. Classified as a diarylethene, it features a central ethylene moiety with one phenyl group substituents on each end of the carboncarbon double bond. It has an (E) stereochemistry, meaning that the phenyl groups are located on opposite sides of the double bond, the opposite of its geometric isomer, cis-stilbene.
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Reactant
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1-Hydroxy-1,2-benziodoxol-3(1H)-one 1-oxide
(Nicolaou IBX dehydrogenation)
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