| Weight | 153.184 g/mol |
|---|---|
| Formula | C11H7N |
| Hydrogen Acceptors | 1 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 2 |
| Rotatable Bonds | 0 |
1-Naphthonitrile (86-53-3, 25551-35-3)
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- Photochemical cycloaddition of two nearly isoenergetic singlet states of 1-naphthonitrile (The Journal of Physical Chemistry, 1980)
- THE ACTION OF GRIGNARD REAGENTS ON 2-METHOXY-1-NAPHTHONITRILE (Journal of Organic Chemistry, 1948)
- Photochemical reactions of aromatic compounds. 27. Stereospecific photocycloaddition of cis- and trans-1-methoxypropenes to 2-naphthonitrile (Journal of Organic Chemistry, 1977)
- The photocycloaddition of 4-methoxy-1-naphthonitrile and 2-methoxy-1-naphthonitrile with acrylonitrile and 3,4-dihydro-2H-pyran: Facile additions in sunlight (Journal of Photochemistry and Photobiology A-chemistry, 1990)
- Acid-catalyzed reactions of 1,4-dihydro-1-methyl-4-oxo-1-naphthonitrile. Self-condensation to a 13-oxapicene derivative (Journal of Organic Chemistry, 1969)
- The synthesis of azocine derivatives by the photocycloaddition of phenols to 1-naphthonitrile and 4-methoxy-1-naphthonitrile (Journal of Photochemistry and Photobiology A-chemistry, 1990)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1=CC=C2C(=C1)C=CC=C2C#N
-
InChIKeyYJMNOKOLADGBKA-UHFFFAOYSA-N
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