2-Azabicyclo[2.2.1]hept-5-en-3-one structure 
             | 
        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 | |
| Name | 2-Azabicyclo[2.2.1]hept-5-en-3-one | 
|---|---|
| Synonym | More Synonyms | 
| Density | 1.2±0.1 g/cm3 | 
|---|---|
| Boiling Point | 319.3±0.0 °C at 760 mmHg | 
| Melting Point | 54-58 °C(lit.) | 
| Molecular Formula | C6H7NO | 
| Molecular Weight | 109.126 | 
| Flash Point | 167.1±9.8 °C | 
| Exact Mass | 109.052765 | 
| PSA | 29.10000 | 
| LogP | -1.22 | 
| Vapour Pressure | 0.0±0.6 mmHg at 25°C | 
| Index of Refraction | 1.546 | 
| Storage condition | Refrigerator | 
| Water Solubility | >1000 g/L (23 ºC) | 
| Symbol | 
                                    
                                     
                                    
                                    GHS07  | 
                            
|---|---|
| Signal Word | Warning | 
| Hazard Statements | H302-H317 | 
| Precautionary Statements | P280 | 
| Personal Protective Equipment | dust mask type N95 (US);Eyeshields;Gloves | 
| Hazard Codes | Xn:Harmful; | 
| Risk Phrases | R22;R43 | 
| Safety Phrases | S26-S36-S36/37 | 
| RIDADR | NONH for all modes of transport | 
| WGK Germany | 1 | 
| HS Code | 2933790090 | 
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                                         ~78%  
                                            2-Azabicyclo[2.... CAS#:49805-30-3  | 
                                
| Literature: Kuraray Co., Ltd. Patent: US6060609 A1, 2000 ; | 
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                                         ~%  
                                            2-Azabicyclo[2.... CAS#:49805-30-3  | 
                                
| Literature: Lonza Ltd. Patent: US5200527 A1, 1993 ; | 
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                                         ~56%  
                                            2-Azabicyclo[2.... CAS#:49805-30-3  | 
                                
| Literature: Heesing, Albert; Herdering, Wilhelm Chemische Berichte, 1983 , vol. 116, # 3 p. 1081 - 1096 | 
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                                         ~%  
                                            2-Azabicyclo[2.... CAS#:49805-30-3  | 
                                
| Literature: Griffiths, Gareth J.; Previdoli, Felix E. Journal of Organic Chemistry, 1993 , vol. 58, # 22 p. 6129 - 6131 | 
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                                            2-Azabicyclo[2.... CAS#:49805-30-3  | 
                                
| Literature: Pham, Phuong-T.; Vince, Robert Phosphorus, Sulfur and Silicon and the Related Elements, 2007 , vol. 182, # 4 p. 779 - 791 | 
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                                         ~%  
                                            2-Azabicyclo[2.... CAS#:49805-30-3  | 
                                
| Literature: Morgan, Paul E.; McCague, Ray; Whiting, Andrew Chemical Communications, 1996 , # 15 p. 1811 - 1812 | 
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                                         ~%  
                                            2-Azabicyclo[2.... CAS#:49805-30-3  | 
                                
| Literature: Katagiri, Nobuya; Makino, Masashi; Tamura, Takahiro; Kaneko, Chikara Chemical and Pharmaceutical Bulletin, 1996 , vol. 44, # 4 p. 850 - 852 | 
| HS Code | 2933790090 | 
|---|---|
| Summary | 2933790090. other lactams. VAT:17.0%. Tax rebate rate:9.0%. . MFN tariff:9.0%. General tariff:20.0% | 
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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 u...  | 
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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 remaine...  | 
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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) 
  | 
                                
| 3-Azabicyclo[2.2.1]hepta-5-ene-2-one | 
| Vince's lactam | 
| 2-Azabicyclo[2.2.1]hept-5-en-3-one, (1R,4S)- | 
| 2-Azabicyclo[2.2.1]hept-5-en-3-one | 
| 2-Arabicyclo[2.2.1]hept-5-en-3-one | 
| MFCD00213364 | 
| 2-Azabicyclo(2,2,1,)hept-5-en-3-on | 
| (+/-)-2-Azabicyclo[2.2.1]hept | 
| EINECS 421-830-3 | 
| T55 A CMV FUTJ | 
| 2-Azabicyclo[2 | 
| 4-Amino-2-cyclopentene-1-carboxylic acid lactam | 
| (1R)-(-)-2-Azabicyclo[2.2.1]hept-5-en-3-one | 
| Azabicyclo[2,2,1]hept-5-en-3-one | 
| 2-Azabicyclo[2.2.1]h | 
| 1]hept-5-en-3-one | 
| Vince lactam | 
| ((1R,4S)-2-Azabicyclo[2.2.1]hept-5-en-3-one | 
| (+/-)-2-azabicyclo[2.2.1]hept-5-en-3-one | 
| (±)-2-Azabicyclo[2.2.1]hept-5-en-3-one |