| Weight | 143.189 g/mol |
|---|---|
| Formula | C10H9N |
| Hydrogen Acceptors | 1 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 2 |
| Rotatable Bonds | 1 |
1-Phenylpyrrole (635-90-5)
N-phenylpyrrole
Score:
#89 in Physical chemistry
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#2180 in Physics
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#6747 in Chemistry
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- METALATION OF PYRROLE, 1-METHYLPYRROLE, AND 1-PHENYLPYRROLE WITH n-BUTYLLITHIUM (Journal of Organic Chemistry, 1955)
- 2-Lithio-1-phenylpyrrole: X-Ray Structure Analysis and 6Li-1H 2D Heteronuclear Overhauser NMR Spectroscopy (2D HOESY) (Angewandte Chemie, 1986)
- N-Phenylpyrrole: a kinetic, though not thermodynamic preference for dilithiation (Tetrahedron, 1993)
- Ligand-activated lithium-mediated zincation of N-phenylpyrrole. (Chemistry: A European Journal, 2007)
- Electronic spectra of jet-cooled 1-phenylpyrrole: Large-amplitude torsional motion and twisted intramolecular charge-transfer phenomenon (Journal of Chemical Physics, 1998)
- Vinylogous carbinolamine tumor inhibitors. 4. Antileukemic activity of derivatives of 1,2-dimethyl-3,4-bis(hydroxymethyl)-5-phenylpyrrole bis(N-methylcarbamate) (Journal of Medicinal Chemistry, 1979)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - N-phenylpyrrole
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SMILESC1=CC=C(C=C1)N2C=CC=C2
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InChIKeyGEZGAZKEOUKLBR-UHFFFAOYSA-N
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1-Phenylpyrrole
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