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Home > Other Heterocycles > 49805-30-3
49805-30-3 | 2-Azabicyclo[2.2.1]hept-5-en-3-one
CAS No: 49805-30-3 Catalog No: AG00334L MDL No:MFCD00213364
Product Description
Catalog Number:
AG00334L
Chemical Name:
2-Azabicyclo[2.2.1]hept-5-en-3-one
CAS Number:
49805-30-3
Molecular Formula:
C6H7NO
Molecular Weight:
109.1259
MDL Number:
MFCD00213364
IUPAC Name:
2-azabicyclo[2.2.1]hept-5-en-3-one
InChI:
InChI=1S/C6H7NO/c8-6-4-1-2-5(3-4)7-6/h1-2,4-5H,3H2,(H,7,8)
InChI Key:
DDUFYKNOXPZZIW-UHFFFAOYSA-N
SMILES:
C1C2C=CC1NC2=O
Properties
Complexity:
162
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
109.053g/mol
Formal Charge:
0
Heavy Atom Count:
8
Hydrogen Bond Acceptor Count:
1
Hydrogen Bond Donor Count:
1
Isotope Atom Count:
0
Molecular Weight:
109.128g/mol
Monoisotopic Mass:
109.053g/mol
Rotatable Bond Count:
0
Topological Polar Surface Area:
29.1A^2
Undefined Atom Stereocenter Count:
2
Undefined Bond Stereocenter Count:
0
XLogP3:
0.1
Literature
| Title | Journal |
|---|---|
| 2-Azabicyclo[2.2.1]hept-5-en-3-one: chemical profile of a versatile synthetic building block and its impact on the development of therapeutics. | Chemical reviews 20120808 |
| Promiscuous enantioselective (-)-γ-lactamase activity in the Pseudomonas fluorescens esterase I. | Organic & biomolecular chemistry 20120507 |
| Synthesis of neplanocin F analogues as potential antiviral agents. | Bioorganic & medicinal chemistry 20061215 |
| Synthesis of carbovir and abacavir from a carbocyclic precursor. | Current protocols in nucleic acid chemistry 20060701 |
| Electronic structure effects of amide group: Vince lactam. | Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy 20050301 |
| First synthesis of 2',3'-epimino-carbocyclic nucleosides. | Organic & biomolecular chemistry 20030207 |
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