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331910

Sigma-Aldrich

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

98%

Synonym(s):

(±)-2-Azabicyclo[2.2.1]hept-5-en-3-one, 4-Amino-2-cyclopentene-1-carboxylic acid lactam

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About This Item

Empirical Formula (Hill Notation):
C6H7NO
CAS Number:
49805-30-3
Molecular Weight:
109.13
Beilstein/REAXYS Number:
508342
MDL number:
MFCD00213364
UNSPSC Code:
12352100
PubChem Substance ID:
24860009
NACRES:
NA.22

Quality Level

100

assay

98%

bp

102-106 °C/0.25 mmHg (lit.)

mp

54-58 °C (lit.)

SMILES string

O=C1N[C@H]2C[C@@H]1C=C2

InChI

1S/C6H7NO/c8-6-4-1-2-5(3-4)7-6/h1-2,4-5H,3H2,(H,7,8)/t4-,5+/m0/s1

InChI key

DDUFYKNOXPZZIW-CRCLSJGQSA-N

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General description

2-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.

Application

2-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

pictograms

Exclamation mark
GHS07

signalword

Warning

hcodes

H302,H317

Hazard Classifications

Acute Tox. 4 Oral - Skin Sens. 1

wgk_germany

WGK 1

flash_point_f

closed cup

flash_point_c

closed cup

ppe

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

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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.
Journal of the Chemical Society. Chemical Communications, 16, 1120-1121 (1990)
Patricia Écija et al.
The journal of physical chemistry. A, 116(41), 10099-10106 (2012-09-19)
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···H(2)O system offers a simple model
Vasu Nair et al.
Molecules (Basel, Switzerland), 18(9), 11576-11585 (2013-09-21)
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 bredinin is described. The key precursor, (3aS,4R,6R,6aR)-6-((methoxy-methoxy)methyl)-2,2-dimethyltetrahydro-3aH-cyclopenta[d][1,3]dioxol-4-amine

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