Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C5H10O |
| Molecular Weight | 86.1323 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CCOCC=C
InChI
InChIKey=OJPSFJLSZZTSDF-UHFFFAOYSA-N
InChI=1S/C5H10O/c1-3-5-6-4-2/h3H,1,4-5H2,2H3
| Molecular Formula | C5H10O |
| Molecular Weight | 86.1323 |
| 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 |
|---|---|---|
| Practical asymmetric approach to medium-sized carbocycles based on the combination of two ru-catalyzed transformations and a lewis Acid-induced cyclization. | 2005-01-20 |
|
| Atom-efficient assembly of 1,5-oxygen-bridged medium-sized carbocycles by sequential combination of a Ru-catalyzed alkyne-alkene coupling and a Prins-type cyclization. | 2002-04-24 |
|
| Facile allylic C-H bond activation on the bridging disulfide ligand in the Ru(III) dinuclear complex having a conjugated RuSSRu core. | 2001-10-22 |
Patents
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 19:03:32 GMT 2025
by
admin
on
Mon Mar 31 19:03:32 GMT 2025
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| Record UNII |
SM8T658RE3
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| Record Status |
Validated (UNII)
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