Details
Stereochemistry | RACEMIC |
Molecular Formula | C7H12O3 |
Molecular Weight | 144.1684 |
Optical Activity | ( + / - ) |
Defined Stereocenters | 0 / 1 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
CCOC(=O)C(C)C(C)=O
InChI
InChIKey=FNENWZWNOPCZGK-UHFFFAOYSA-N
InChI=1S/C7H12O3/c1-4-10-7(9)5(2)6(3)8/h5H,4H2,1-3H3
Approval Year
PubMed
Title | Date | PubMed |
---|---|---|
Stereochemical consequences of threefold symmetry in asymmetric catalysis: distorting C3 Chiral 1,1,1-tris(oxazolinyl)ethanes ("trisox") in CuII Lewis acid catalysts. | 2007 |
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[Effects of allelochemical EMA from reed on the production and release of cyanotoxins in Microcystis aeruginosa]. | 2007 Sep |
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3,4-Dimethyl-1H-1,2,4-triazepino[2,3-a]benzimidazol-2(3H)-one. | 2010 Apr 17 |
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Enhancement effect of ethyl-2-methyl acetoacetate on triacylglycerols production by a freshwater microalga, Scenedesmus sp. LX1. | 2010 Dec |
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210-179-9
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1102
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701
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DTXSID2033493
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NE9WOZ20JE
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609-14-3
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1522-45-8
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ALTERNATIVE |
SUBSTANCE RECORD