Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Infobox references
Chemical compound
Norcamphor is an organic compound, classified as a bicyclic ketone. It is an analog of camphor, but without the three methyl groups. A colorless solid, it is used as a building block in organic synthesis. Norcamphor is prepared from norbornene via the 2-formate ester, which is oxidized. It is a useful precursor to norborneols.[2]
^ ab"Norcamphor". Sigma-Aldrich. Retrieved March 11, 2013.
^Kleinfelter, Donald C.; Schleyer, Paul von R. (1962). "2-Norbornanone". Org. Synth. 42: 79. doi:10.15227/orgsyn.042.0079.
Norcamphor is an organic compound, classified as a bicyclic ketone. It is an analog of camphor, but without the three methyl groups. A colorless solid...
hydrocarbons. The compound was originally synthesized by reduction of norcamphor. The name norbornane is derived from bornane, which is 1,7,7-trimethylnorbornane...
tetrafluoroborate salt of 2-quinuclidone is a six-step affair starting from norcamphor the final step being an azide - ketone Schmidt reaction (38% yield): This...
C7H10O (molar mass: 110.15 g/mol, exact mass: 110.0732 u) may refer to: Norcamphor Tetrahydrobenzaldehyde, or 1,2,3,6-Tetrahydrobenzaldehyde This set index...
expansions. I. Diazomethane and Tiffeneau-Demjanov ring expansions of norcamphor and dehydronorcamphor". J. Org. Chem. 38 (23): 4059. doi:10.1021/jo00987a023...