(+)-10,2-Camphorsultam
CAS: 108448-77-7
Ref. 3D-FC59960
| 2g | A consultar | ||
| 5g | A consultar | ||
| 10g | A consultar | ||
| 25g | A consultar | ||
| 50g | A consultar |
Información del producto
- (2S)-Bornane-10,2-sultam(1R,5S)-10,10-Dimethyl-3-thia-4-azatricyclo[5.2.1.01,5]decane 3,3-Dioxide
- [3aR-(3aalpha,6alpha,7abeta)]-Hexahydro-8,8-dimethyl-3H-3a,6-methano-2,1-benzisothiazole 2,2-dioxide
- (1R)-(+)-2,10-Camphorsultam
- (1R)-(+)-2,10,Camphor sultam
- 8,8-Dimethylhexahydro-3A,6-Methano-2,1-Benzothiazole 2,2-Dioxide
- (3aR,6S,7aS)-8,8-dimethylhexahydro-3a,6-methano-2,1-benzothiazole 2,2-dioxide
- (3aR,6R,7aR)-8,8-dimethylhexahydro-3a,6-methano-2,1-benzisothiazole 2,2-dioxide
- (+)-Camphorsultam
(+)-10,2-Camphorsultam is an isoxazolidine of the l-glutamic acid type. It has a chiral carbon atom and, in addition to the usual carboxyl group, has an amino group. The enantiomers of (+)-10,2-camphorsultam are made in a stereoselective manner by using potassium carbonate as a catalyst. This compound can be used for synthesis reactions such as aminations, enantiomer separations, and cycloadditions. In addition to this it functions as a chiral auxiliary in 1,3-dipolar cycloadditions with carbonyl derivatives.
Propiedades químicas
Consulta técnica sobre: 3D-FC59960 (+)-10,2-Camphorsultam
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