Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C6H10O2 |
| Molecular Weight | 114.1424 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CCC(=O)OCC=C
InChI
InChIKey=XRFWKHVQMACVTA-UHFFFAOYSA-N
InChI=1S/C6H10O2/c1-3-5-8-6(7)4-2/h3H,1,4-5H2,2H3
| Molecular Formula | C6H10O2 |
| Molecular Weight | 114.1424 |
| 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 |
|---|---|---|
| Enantioselective carbonyl allylation, crotylation, and tert-prenylation of furan methanols and furfurals via iridium-catalyzed transfer hydrogenation. | 2010-03-05 |
|
| anti-Diastereo- and enantioselective carbonyl crotylation from the alcohol or aldehyde oxidation level employing a cyclometallated iridium catalyst: alpha-methyl allyl acetate as a surrogate to preformed crotylmetal reagents. | 2009-02-25 |
Patents
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 18:40:04 GMT 2025
by
admin
on
Mon Mar 31 18:40:04 GMT 2025
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| Record UNII |
0OYW8C5029
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| Record Status |
Validated (UNII)
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CFR |
21 CFR 172.515
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JECFA EVALUATION |
ALLYL PROPIONATE
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538
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61319
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0OYW8C5029
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219-307-8
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2408-20-0
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DTXSID0047668
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