(+)-3-Bromocamphor
CAS: 10293-06-8
Ref. 3D-FB63284
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Información del producto
- endo-3-Bromo-D-camphor(1R-endo)-3-Bromo-1,7,7-trimethylbicyclo[2.2.1]heptan-2-one
- ((1R)-endo)-(+)-3-bromocamphor
- (+)-endo-3-Bromocamphor
- (1R)-3-bromo-1,7,7-trimethylbicyclo[2.2.1]heptan-2-one
- (1R,3R,4R)-3-bromo-1,7,7-trimethylbicyclo[2.2.1]heptan-2-one
- (1R,3S)-3-bromo-1,7,7-trimethylbicyclo[2.2.1]heptan-2-one
- (1R,3S,4S)-3-bromo-1,7,7-trimethylbicyclo[2.2.1]heptan-2-one
- (1R-Endo)-3-Bromo-1,7,7-Trimethylbicyclo[2.2.1]Heptan-2-One
- (1S,3R,4R)-3-bromo-1,7,7-trimethylbicyclo[2.2.1]heptan-2-one
- (IR)endo-(+)-3-bromoCamphor
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- 1R)-?+?3-Bromo Camphor, 98% min
- 2-Bornanone, 3-bromo-, (1R,3S,4S)-(+)-
- Bicyclo[2.2.1]heptan-2-one, 3-bromo-1,7,7-trimethyl-, (1R,3S,4S)-
- Bicyclo[2.2.1]heptan-2-one, 3-bromo-1,7,7-trimethyl-, (1R-endo)-
- Bromocamphor,98%
- Camphor, 3α-bromo-, (+)-
- endo-(+)-3-Bromo-2-bornanone
(+)-3-Bromocamphor is an organic compound that belongs to the class of ethylene diamines. It is a colorless, odorless solid that can be prepared by debromination of camphor with phosphorus pentachloride and sodium carbonate in water. The molecule can be decomposed by amines, easily forming the skeleton. (+)-3-Bromocamphor has been shown to have low energy transfer reactions and low symmetry; thus, it can be used for asymmetric synthesis.
Propiedades químicas
Consulta técnica sobre: 3D-FB63284 (+)-3-Bromocamphor
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