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

2-Azabicyclo[2.2.1]hept-5-en-3-one
  • CAS No.:49805-30-3
Other grades of this product :
2-Azabicyclo[2.2.1]hept-5-en-3-one Basic information
Product Name:2-Azabicyclo[2.2.1]hept-5-en-3-one
Synonyms:(+/-)-2-Azabicyclo[2.2.1]hept-;2-AZABICYCLO(2.2.1)HEPT-5-EN-3-ONE, (VINCE LACTAM);2-Azabicyclo(2,2,1,)hept-5-en-3-on;Vince Lactam (2-azabicyclo[2.2.1]hept-5-en-3-one);2-AZABICYCLO(2.2.1)HEPT-5-EN-3-ONE, 99% (VINCE LACTAM);(±)-2-Azabicyclo[2.2.1]hept-5-en-3-one, 4-Amino-2-cyclopentene-1-carboxylic acid lactam;3-Azabicyclo[2.2.1]hepta-5-ene-2-one;(±)-2-Azabicyclo[2.2.1]hept-5-en-3-one,98%
CAS:49805-30-3
MF:C6H7NO
MW:109.13
EINECS:421-830-3
Product Categories:Cyanogen chloride derivatives;Hydrocyanic acid derivatives;(intermediate of abacavir);Heterocycles;Intermediates;Fused Ring Systems;3
Mol File:49805-30-3.mol
2-Azabicyclo[2.2.1]hept-5-en-3-one Chemical Properties
Melting point 54-58 °C(lit.)
Boiling point 102-106 °C0.25 mm Hg(lit.)
density 1.1143 (rough estimate)
vapor pressure 0.3-1.06Pa at 25-40℃
refractive index 1.5040 (estimate)
Fp >230 °F
storage temp. Keep in dark place,Sealed in dry,Room Temperature
solubility soluble in Methanol
pka15.48±0.20(Predicted)
form Crystalline Powder
color Off-white to beige
Water Solubility >1000 g/L (23 ºC)
BRN 508342
InChIKeyDDUFYKNOXPZZIW-UHFFFAOYSA-N
LogP-0.14 at 20℃
Surface tension69.9mN/m at 1g/L and 20℃
CAS DataBase Reference49805-30-3(CAS DataBase Reference)
Safety Information
Hazard Codes Xi,Xn
Risk Statements 36/37/38-43-22
Safety Statements 26-36-36/37
WGK Germany 1
HS Code 29337900
MSDS Information
ProviderLanguage
SigmaAldrich English
ACROS English
2-Azabicyclo[2.2.1]hept-5-en-3-one Usage And Synthesis
Chemical Propertiessolid
UsesIntermediate for pharmaceuticals. Product Data Sheet
Uses2-Azabicyclo[2.2.1]hept-5-en-3-one was used in:
  • preparation of (3aS,4R,6R,6aR)-6-((methoxy-methoxy)methyl)-2,2-dimethyltetrahydro-3aH-cyclopenta[d][1,3]dioxol-4-amine, a precursor of analog of bredinin
  • synthesis of therapeutic drugs
  • chemoenzymatic synthesis of (?)-carbovir
UsesAbacavir intermediate. 2-Azabicyclo[2.2.1]hept-5-en-3-one is used as an intermediate in the synthesis of carbocyclic sugar amines, carbanucleosides, and carbocyclic dinucleotide analogues.
General Description2-Azabicyclo[2.2.1]hept-5-en-3-one is also referred as vince lactam. It is a versatile intermediate in the synthesis of carbocyclic nucleosides. 2-Azabicyclo[2.2.1]hept-5-en-3-one and its monohydrated complex was investigated in a supersonic jet by Fourier transform microwave spectroscopy.

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