Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C5H8O |
| Molecular Weight | 84.1164 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CC(=O)C1CC1
InChI
InChIKey=HVCFCNAITDHQFX-UHFFFAOYSA-N
InChI=1S/C5H8O/c1-4(6)5-2-3-5/h5H,2-3H2,1H3
| Molecular Formula | C5H8O |
| Molecular Weight | 84.1164 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Synthesis and reactivity of six-membered oxa-nickelacycles: a ring-opening reaction of cyclopropyl ketones. | 2009-10-05 |
|
| (Z)- and (E)-2-(1,2-dihydroxyethyl)methylenecyclopropane analogues of 2'-deoxyadenosine and 2'-deoxyguanosine. Synthesis of all stereoisomers, absolute configuration, and antiviral activity. | 2009-05-28 |
|
| Synthesis of spiropyrans: H-abstractions in 3-cycloalkenyloxybenzopyrans. | 2007-03-21 |
|
| Synthesis of 1,2,4-trioxepanes and 1,2,4-trioxocanes via photooxygenation of homoallylic alcohols. | 2006-11-24 |
|
| Designing the "search pathway" in the development of a new class of highly efficient stereoselective hydrosilylation catalysts. | 2005-04-22 |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 23:22:49 GMT 2025
by
admin
on
Mon Mar 31 23:22:49 GMT 2025
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| Record UNII |
N27YY1XCFH
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| Record Status |
Validated (UNII)
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| Record Version |
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N27YY1XCFH
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DTXSID9074854
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1940
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