Details
Stereochemistry | ACHIRAL |
Molecular Formula | C5H8O2 |
Molecular Weight | 100.1158 |
Optical Activity | NONE |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 1 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
CC\C=C\C(O)=O
InChI
InChIKey=YIYBQIKDCADOSF-ONEGZZNKSA-N
InChI=1S/C5H8O2/c1-2-3-4-5(6)7/h3-4H,2H2,1H3,(H,6,7)/b4-3+
Molecular Formula | C5H8O2 |
Molecular Weight | 100.1158 |
Charge | 0 |
Count |
|
Stereochemistry | ACHIRAL |
Additional Stereochemistry | No |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 1 |
Optical Activity | NONE |
Approval Year
PubMed
Title | Date | PubMed |
---|---|---|
Intramolecularly competitive Ireland-Claisen rearrangements: scope and potential applications to natural product synthesis. | 2002 Apr 5 |
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Asymmetric total synthesis of bacillariolide III, a marine oxylipin. | 2004 Feb 5 |
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Efficient synthesis of a trisubstituted 1,6-naphthyridone from acetonedicarboxylate and regioselective Suzuki arylation. | 2005 Dec 9 |
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Conjugate additions of Me2CuLi to enantiopure gamma-hydroxy-delta-sulfinyl and sulfonyl pentenoates. | 2005 Nov 25 |
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Pentenoic acid pathways for cellulosic biofuels. | 2010 Jun 14 |
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Extension of the PNA world by functionalized PNA monomers eligible candidates for inverse Diels Alder Click Chemistry. | 2010 Jun 27 |
|
A new labdanic norditerpene from Pinus sylvestris. | 2010 Oct |
Substance Class |
Chemical
Created
by
admin
on
Edited
Fri Dec 15 17:55:18 GMT 2023
by
admin
on
Fri Dec 15 17:55:18 GMT 2023
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Record UNII |
1RG66883CF
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Record Status |
Validated (UNII)
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Record Version |
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