| Weight | 168.199 g/mol |
|---|---|
| Formula | C11H8N2 |
| Hydrogen Acceptors | 1 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 3 |
| Rotatable Bonds | 0 |
1h-pyrrolo[3,2-h]quinoline (233-88-5)
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- Excited-State Proton Transfer through Water Bridges and Structure of Hydrogen-Bonded Complexes in 1H-Pyrrolo(3,2-h)quinoline: Adiabatic Time-Dependent Density Functional Theory Study (Journal of Physical Chemistry A, 2006)
- Role of Ground State Structure in Photoinduced Tautomerization in Bifunctional Proton DonorAcceptor Molecules: 1H-Pyrrolo[3,2-h]quinoline and Related Compounds (Journal of the American Chemical Society, 1999)
- Fluorescence quenching in cyclic hydrogen-bonded complexes of 1H-pyrrolo[3,2-h]quinoline with methanol: cluster size effect (Physical Chemistry Chemical Physics, 2007)
- Separation of Different Hydrogen-Bonded Clusters by Femtosecond UV-Ionization-Detected Infrared Spectroscopy: 1H-Pyrrolo[3,2-h]quinoline(H2O)n=1,2 Complexes (Journal of Physical Chemistry A, 2008)
- Photoinduced double proton transfer in water complexes of 1H-pyrrolo[3,2-h]quinoline and dipyrido[2,3-a:3', 2'-i]carbazole (Chemical Physics Letters, 2002)
- Theoretical study on excited-state intermolecular proton transfer reactions of 1H-pyrrolo[3,2-h]quinoline with water and methanol (Theoretical Chemistry Accounts, 2013)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1=CC2=C(C3=C(C=C2)C=CN3)N=C1
-
InChIKeyWNCAJASYDRNBHG-UHFFFAOYSA-N
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