| Weight | 125.171 g/mol |
|---|---|
| Formula | C7H11NO |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 0 |
8-azabicyclo[3.2.1]octan-3-one (5632-84-8)
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- TOTAL SYNTHESIS OF (+)-MONOMORINE I VIA ASYMMETRIC -KETONIC CLEAVAGE OF 8-AZABICYCLO[3.2.1]OCTAN-3-ONE (Chemical & Pharmaceutical Bulletin, 1990)
- Synthesis and Polymerization of an Optically Active Bicyclic Oxalactam. A Novel Hydrophilic Polyamide Membrane Prepared from (+)-(1R,5S)-8-Oxa-6-azabicyclo[3.2.1]octan-7-one (Macromolecules, 1980)
- Synthetic carbapenem antibiotics II. Stereoisomers of 7-hydroxyethyl-2,2,5-trimethyl-3-oxa-1-azabicyclo[4.2.O]octan-8-one (Tetrahedron Letters, 1985)
- Synthesis and polymerization of 8OXA6azabicyclo[3.2.1] octan7one (Journal of Polymer Science: Polymer Letters Edition, 1973)
- Nuclear analogs of .beta.-lactam antibiotics. 6. 3-Oxa-1-azabicyclo[4.2.0]octan-8-one-2-carboxylic acids (Journal of the American Chemical Society, 1979)
- Crystal Structures of 8-Oxa-6-azabicyclo[3.2.1]octan-7-one and the 4(e)-Bromo-substituted Derivative (Bulletin of the Chemical Society of Japan, 1986)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1CC2CC(=O)CC1N2
-
InChIKeyCVDLBKMNONQOHJ-UHFFFAOYSA-N
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