Identification | Back Directory | [Name]
(N-CROTONYL)-(2R)-BORNANE-10,2-SULTAM | [CAS]
94668-55-0 | [Synonyms]
(1S)-N-crotyl-2,10-camphorsultam (N-CROTONYL)-(2R)-BORNANE-10,2-SULTAM (R)-(-)-(2-BUTENOYL)-2,10-CAMPHORSULTAM (E)-1-((3aS,6R,7aR)-8,8-Dimethyl-2,2-dioxidohexahydro-1H-3a,6-methanobenzo[c]isothiazol-1-yl)but-2-en-1-one 2-Buten-1-one, 1-[(3aS,6R,7aR)-tetrahydro-8,8-dimethyl-2,2-dioxido-3H-3a,6-methano-2,1-benzisothiazol-1(4H)-yl]-, (2E)- (N-Crotonyl)-(2R)-bornane-10,2-sultam, (2E)-1-[(3aS,6R,7aR)-Tetrahydro-8,8-dimethyl-2,2-dioxido-3H-3a,6-methano-2,1-benzisothiazol-1(4H)-yl]-2-buten-1-one | [Molecular Formula]
C14H21NO3S | [MDL Number]
MFCD00269664 | [MOL File]
94668-55-0.mol | [Molecular Weight]
283.39 |
Chemical Properties | Back Directory | [Melting point ]
180-184 °C(lit.) | [Boiling point ]
397.2±25.0 °C(Predicted) | [density ]
1.27±0.1 g/cm3(Predicted) | [pka]
-14.19±0.40(Predicted) | [optical activity]
[α]24/D 100°, c = 1 in ethanol |
Hazard Information | Back Directory | [Uses]
(R)-(-)-(2-Butenoyl)-2,10-camphorsultam can be used:
- In the asymmetric total synthesis of lycopodine via diastereoselective cyclization and intramolecular Mannich cyclization.
- To prepare (S)-4,4-dichloro-3-methylbutanoic acid, which is utilized as a key intermediate for the total synthesis of dysideaproline E.
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