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2-Azabicyclo[2.2.1]hept-5-en-3-one

Names

[ CAS No. ]:
49805-30-3

[ Name ]:
2-Azabicyclo[2.2.1]hept-5-en-3-one

[Synonym ]:
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

Chemical & Physical Properties

[ 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)

MSDS

Safety Information

[ 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

Synthetic Route

Customs

[ HS Code ]: 2933790090

[ Summary ]:
2933790090. other lactams. VAT:17.0%. Tax rebate rate:9.0%. . MFN tariff:9.0%. General tariff:20.0%

Articles

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...

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...

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)


More Articles


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