Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C4H8O |
| Molecular Weight | 72.1057 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
COC(C)=C
InChI
InChIKey=YOWQWFMSQCOSBA-UHFFFAOYSA-N
InChI=1S/C4H8O/c1-4(2)5-3/h1H2,2-3H3
| Molecular Formula | C4H8O |
| Molecular Weight | 72.1057 |
| 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 |
|---|---|---|
| Glycosyl hydroperoxides derived from 2-deoxysugars. | 2010-11-22 |
|
| Acetonation of L-pentoses and 6-deoxy-L-hexoses under kinetic control using heterogeneous acid catalysts. | 2010-07-19 |
|
| Preparation of pure lipid hydroperoxides. | 2008-12 |
|
| Identification of the aromatic tertiary N-oxide functionality in protonated analytes via ion/molecule reactions in mass spectrometers. | 2008-07-04 |
|
| Mechanism and chemoselectivity of the Pd(II)-catalyzed allylation of aldehydes: a density functional theory study. | 2007-02-02 |
|
| Exclusive formation of alpha-methyleneoxetanes in ketene-alkene cycloadditions. Evidence for intervention of both an alpha-methyleneoxetane and the subsequent 1,4-zwitterion. | 2003-11-26 |
|
| Asymmetric catalysis of hetero-ene reactions with tridentate Schiff base chromium(III) complexes. | 2002-03-27 |
|
| Mixed acetals of cyclodextrins. Preparation of hexakis-, heptakis- and octakis[2,6-di-O-(methoxydimethyl)methyl]-alpha-, beta- and gamma-cyclodextrins. | 2002-02-05 |
|
| A new mixed acetal-type substitution pattern for alpha-cyclodextrin. Preparation of hexakis (3-O-benzyl)- alpha-cyclodextrin. | 2001 |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 19:52:03 GMT 2025
by
admin
on
Mon Mar 31 19:52:03 GMT 2025
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| Record UNII |
15WBG0JT6B
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| Record Status |
Validated (UNII)
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| Record Version |
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8300
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C534882
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116-11-0
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m7343
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15WBG0JT6B
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2-METHOXYPROPENE
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204-125-3
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