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 |
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Stereochemistry | ACHIRAL |
Additional Stereochemistry | No |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Optical Activity | NONE |
Approval Year
PubMed
Title | Date | PubMed |
---|---|---|
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 Feb 25 |
|
Enantioselective carbonyl allylation, crotylation, and tert-prenylation of furan methanols and furfurals via iridium-catalyzed transfer hydrogenation. | 2010 Mar 5 |
Patents
Substance Class |
Chemical
Created
by
admin
on
Edited
Fri Dec 15 17:04:18 GMT 2023
by
admin
on
Fri Dec 15 17:04:18 GMT 2023
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Record UNII |
0OYW8C5029
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Record Status |
Validated (UNII)
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Record Version |
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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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219-307-8
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2408-20-0
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DTXSID0047668
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