Details
| Stereochemistry | RACEMIC |
| Molecular Formula | C6H10O |
| Molecular Weight | 98.143 |
| Optical Activity | ( + / - ) |
| Defined Stereocenters | 0 / 1 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
OC(CC=C)C=C
InChI
InChIKey=SZYLTIUVWARXOO-UHFFFAOYSA-N
InChI=1S/C6H10O/c1-3-5-6(7)4-2/h3-4,6-7H,1-2,5H2
| Molecular Formula | C6H10O |
| Molecular Weight | 98.143 |
| Charge | 0 |
| Count |
|
| Stereochemistry | RACEMIC |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 1 |
| E/Z Centers | 0 |
| Optical Activity | ( + / - ) |
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Regioselective cross-metathesis reaction induced by steric hindrance. | 2004-09-30 |
|
| Enantioselective total synthesis of (+)-rogioloxepane A. | 2003-08-21 |
|
| Concerted rearrangement versus heterolytic cleavage in anionic [2,3]- and [3,3]-sigmatropic shifts. A DFT study of relationships among anion stabilities, mechanisms, and rates. | 2003-03-21 |
|
| The anionic oxy-Cope rearrangement: using chemical reactivity to reveal the facile isomerization of the parent substrates in the gas phase. | 2001-11-02 |
Patents
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 23:12:25 GMT 2025
by
admin
on
Mon Mar 31 23:12:25 GMT 2025
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| Record UNII |
C38864PH9K
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| Record Status |
Validated (UNII)
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| Record Version |
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| Related Record | Type | Details | ||
|---|---|---|---|---|
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ENANTIOMER -> RACEMATE | |||
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ENANTIOMER -> RACEMATE |