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Home > Other Heterocycles > 278-30-8
278-30-8 | Bicyclo[4.2.0]octane
CAS No: 278-30-8 Catalog No: AG002US9 MDL No:
Product Description
Catalog Number:
AG002US9
Chemical Name:
Bicyclo[4.2.0]octane
CAS Number:
278-30-8
Molecular Formula:
C8H14
Molecular Weight:
110.1968
IUPAC Name:
bicyclo[4.2.0]octane
InChI:
InChI=1S/C8H14/c1-2-4-8-6-5-7(8)3-1/h7-8H,1-6H2
InChI Key:
RPZUBXWEQBPUJR-UHFFFAOYSA-N
SMILES:
C1CCC2C(C1)CC2
Properties
Complexity:
74
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
110.11g/mol
Formal Charge:
0
Heavy Atom Count:
8
Hydrogen Bond Acceptor Count:
0
Hydrogen Bond Donor Count:
0
Isotope Atom Count:
0
Molecular Weight:
110.2g/mol
Monoisotopic Mass:
110.11g/mol
Rotatable Bond Count:
0
Topological Polar Surface Area:
0A^2
Undefined Atom Stereocenter Count:
2
Undefined Bond Stereocenter Count:
0
XLogP3:
3.5
Literature
| Title | Journal |
|---|---|
| Synthesis of a new class of aminocyclitol analogues with the conduramine D-2 configuration. | Beilstein journal of organic chemistry 20100101 |
| Evolution of a synthetic strategy: total synthesis of (+/-)-welwitindolinone A isonitrile. | Journal of the American Chemical Society 20080213 |
| Dihalocarbene insertion reactions into C-H bonds of compounds containing small rings: mechanisms and regio- and stereoselectivities. | The Journal of organic chemistry 20071026 |
| Biomimetic synthesis of elysiapyrones A and B. | Organic letters 20050707 |
| Elysiapyrones from Elysia diomedea. Do such metabolites evidence an enzymatically assisted electrocyclization cascade for the biosynthesis of their bicyclo[4.2.0]octane core? | Organic letters 20050203 |
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