(2S)-N-[(1S)-1-(Hydroxydiphenylmethyl)-3-methylbutyl]-2-pyrrolidinecarboxamide
Modify Date: 2024-09-05 16:28:01
![(2S)-N-[(1S)-1-(Hydroxydiphenylmethyl)-3-methylbutyl]-2-pyrrolidinecarboxamide Structure](https://image.chemsrc.com/caspic/290/910110-45-1.png)
(2S)-N-[(1S)-1-(Hydroxydiphenylmethyl)-3-methylbutyl]-2-pyrrolidinecarboxamide structure
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Common Name | (2S)-N-[(1S)-1-(Hydroxydiphenylmethyl)-3-methylbutyl]-2-pyrrolidinecarboxamide | ||
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| CAS Number | 910110-45-1 | Molecular Weight | 366.496 | |
| Density | 1.1±0.1 g/cm3 | Boiling Point | 601.8±55.0 °C at 760 mmHg | |
| Molecular Formula | C23H30N2O2 | Melting Point | 193 °C | |
| MSDS | USA | Flash Point | 317.8±31.5 °C | |
| Name | N-[(2S)-1-Hydroxy-4-methyl-1,1-diphenyl-2-pentanyl]-L-prolinamide |
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| Synonym | More Synonyms |
| Density | 1.1±0.1 g/cm3 |
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| Boiling Point | 601.8±55.0 °C at 760 mmHg |
| Melting Point | 193 °C |
| Molecular Formula | C23H30N2O2 |
| Molecular Weight | 366.496 |
| Flash Point | 317.8±31.5 °C |
| Exact Mass | 366.230713 |
| LogP | 3.63 |
| Vapour Pressure | 0.0±1.8 mmHg at 25°C |
| Index of Refraction | 1.566 |
| RIDADR | NONH for all modes of transport |
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Highly enantioselective direct aldol reaction catalyzed by organic molecules.
Org. Lett. 8 , 4097-4099, (2006) We have demonstrated that a new class of l-proline-based organic compounds catalyzed the direct aldol reaction between aldehydes and acetone to provide beta-hydroxy ketones in good yields. The reactio... |
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Direction of Kinetically versus Thermodynamically Controlled Organocatalysis and Its Application in Chemoenzymatic Synthesis Rulli, G., et al.
Angew. Chem. Int. Ed. Engl. 50 , 1-5, (2011)
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| N-[(2S)-1-Hydroxy-4-methyl-1,1-diphenyl-2-pentanyl]-L-prolinamide |
| 2-Pyrrolidinecarboxamide, N-[(1S)-1-(hydroxydiphenylmethyl)-3-methylbutyl]-, (2S)- |