| Identification | Back Directory | [Name]
(4S,5R)-(-)-4-i-propyl-5-(3,3,4,4,5,5,6,6,7,7,8,8,8-tridecafluorooctyl)-2-oxazolidinone,99% | [CAS]
871210-22-9 | [Synonyms]
(4S,5R)-(-)-4-i-propyl-5-(3,3,4,4,5,5,6,6,7,7,8,8,8-tridecafluorooctyl)-2-oxazolidinone,99%
(4S,5R)-(-)-4-i-Propyl-5-(3,3,4,4,5,5,6,6,7,7,8,8,8-tridecafluorooctyl)-2-oxazolidinone, 99%
(4S,5R)-(-)-4-i-Propyl-5-(3,3,4,4,5,5,6,6,7,7,8,8,8-tridecafluorooctyl)
-2-oxazolidinone, 99% | [Molecular Formula]
C14H14F13NO2 | [MDL Number]
MFCD09834834 | [MOL File]
871210-22-9.mol | [Molecular Weight]
475.25 |
| Chemical Properties | Back Directory | [Melting point ]
96-99°C | [alpha ]
-46° (c 0.43, CHCl3) | [Boiling point ]
344.7±37.0 °C(Predicted) | [density ]
1.430±0.06 g/cm3(Predicted) | [form ]
Powder | [pka]
12.51±0.60(Predicted) | [color ]
white | [EPA Substance Registry System]
(4S,5R)-4-(Propan-2-yl)-5-(3,3,4,4,5,5,6,6,7,7,8,8,8-tridecafluorooctyl)-1,3-oxazolidin-2-one (871210-22-9) |
| Questions And Answer | Back Directory | [Uses]
A chiral fluorous support for conventional and high-throughput organic synthesis. Induces high stereoselectivity in aldol reactions, cycloadditions, conjugate additions and a variety of other reactions of N-acyl derivatives. The fluorous chain permits rapid and efficient isolation of products by solid phase extraction, using only minimal amounts of common solvents.Class of catalytic ligands which when used with a reducing agent, exhibit enantioselectivity in the reduction of a wide range of substrates.
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