2-Azabicyclo[2.2.1]hept-5-en-3-one
![2-Azabicyclo[2.2.1]hept-5-en-3-one Structure](https://image.chemsrc.com/caspic/088/49805-30-3.png)
2-Azabicyclo[2.2.1]hept-5-en-3-one structure
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Common Name | 2-Azabicyclo[2.2.1]hept-5-en-3-one | ||
|---|---|---|---|---|
| CAS Number | 49805-30-3 | Molecular Weight | 109.126 | |
| Density | 1.2±0.1 g/cm3 | Boiling Point | 319.3±0.0 °C at 760 mmHg | |
| Molecular Formula | C6H7NO | Melting Point | 54-58 °C(lit.) | |
| MSDS | Chinese USA | Flash Point | 167.1±9.8 °C | |
| Symbol |
GHS07 |
Signal Word | Warning | |
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Single hydration of the peptide bond: the case of the Vince lactam.
J. Phys. Chem. A 116(41) , 10099-106, (2012) 2-Azabicyclo[2.2.1]hept-5-en-3-one (ABH or Vince lactam) and its monohydrated complex (ABH···H(2)O) have been observed in a supersonic jet by Fourier transform microwave spectroscopy. ABH is broadly used in the synthesis of therapeutic drugs, whereas the ABH·... |
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Synthesis of a novel carbocyclic analog of bredinin.
Molecules 18(9) , 11576-85, (2013) The natural nucleoside antibiotic, bredinin, exhibits antiviral and other biological activities. While various nucleosides related to bredinin have been synthesized, its carbocyclic analog has remained unknown. Synthesis of this heretofore unknown analog of b... |
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Chemoenzymatic synthesis of (-)-carbovir utilizing a whole cell catalysed resolution of 2-azabicyclo [2.2. 1] hept-5-en-3-one. Steven, J. C.
J. Chem. Soc. Chem. Commun. 16 , 1120-21, (1990)
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