| Weight | 149.149 g/mol |
|---|---|
| Formula | C8H7NO2 |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 2 |
4-Nitrostyrene (100-13-0)
Score:
#2226 in Physics
,
#6879 in Chemistry
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- Prevention of Platelet Glycoprotein IIb/IIIa Activation by 3,4-Methylenedioxy--Nitrostyrene, A Novel Tyrosine Kinase Inhibitor (Molecular Pharmacology, 2006)
- 3,4-Methylenedioxy--nitrostyrene Inhibits NLRP3 Inflammasome Activation by Blocking Assembly of the Inflammasome (Journal of Biological Chemistry, 2014)
- A new class of chiral pyrrolidine for asymmetric Michael addition reactions. New mechanism via simple 4+2 type attack of the enamine on the trans-nitrostyrene (Tetrahedron, 2007)
- Ab initio time-dependent coupled perturbed Hartree-Fock studies of optical nonlinearities of organic molecules: alkyl derivatives of 4-amino-.beta.-nitrostyrene (The Journal of Physical Chemistry, 1993)
- Promiscuous Catalysis of Asymmetric Michael-Type Additions of Linear Aldehydes to -Nitrostyrene by the Proline-Based Enzyme 4-Oxalocrotonate Tautomerase (ChemBioChem, 2013)
- 3,4-Methylenedioxy--nitrostyrene inhibits adhesion and migration of human triple-negative breast cancer cells by suppressing 1 integrin function and surface protein disulfide isomerase (Biochimie, 2015)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC=CC1=CC=C(C=C1)[N+](=O)[O-]
-
InChIKeyYFZHODLXYNDBSM-UHFFFAOYSA-N
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Synthesis
Reactant
+
1-Hydroxy-1,2-benziodoxol-3(1H)-one 1-oxide
(Nicolaou IBX dehydrogenation)
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4-Nitrostyrene
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