| Weight | 147.177 g/mol |
|---|---|
| Formula | C9H9NO |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 0 |
1-Indanone oxime (68253-35-0)
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- Beckmann Rearrangements of 1-Indanone Oxime Derivatives Using Aluminum Chloride and Mechanistic Considerations (Bulletin of The Korean Chemical Society, 2000)
- Studies on the Syntheses of Heterocyclic Compounds. CLIX. The Reaction of 2-Nitro-1-indanone Oxime with Formalin and Hydrochloric Acid (Chemical & Pharmaceutical Bulletin, 1966)
- Beckmann Rearrangement of 1-Indanone Oxime Using Aluminum Chloride (Bulletin of The Korean Chemical Society, 1998)
- 736. Indene and related compounds. Part III. Ring expansion of 2-nitro-1-indanone oxime to isocarbostyril derivatives (Journal of The Chemical Society (resumed), 1964)
- [Indene and related compounds. V. Ring expansion of 2-nitro-1-indanone oxime with polyphosphoric acid. (Studies on the syntheses of heterocyclic compounds. 173.)]. (Yakugaku Zasshi-journal of The Pharmaceutical Society of Japan, 1967)
- ChemInform Abstract: Beckmann Rearrangements of 1-Indanone Oxime Derivatives Using Aluminum Chloride and Mechanistic Considerations. (ChemInform, 2001)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1CC(=NO)C2=CC=CC=C21
-
InChIKeyATEGUFMEFAGONB-UHFFFAOYSA-N
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