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
| Molecular Formula | C7H12O3 |
| Molecular Weight | 144.1684 |
| Charge | 0 |
| Count |
|
| Stereochemistry | RACEMIC |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 1 |
| E/Z Centers | 0 |
| Optical Activity | ( + / - ) |
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Enhancement effect of ethyl-2-methyl acetoacetate on triacylglycerols production by a freshwater microalga, Scenedesmus sp. LX1. | 2010-12 |
|
| Environmentally benign periphyton bioreactors for controlling cyanobacterial growth. | 2010-12 |
|
| 3,4-Dimethyl-1H-1,2,4-triazepino[2,3-a]benzimidazol-2(3H)-one. | 2010-04-17 |
|
| Effects of a novel allelochemical ethyl 2-methyl acetoacetate (EMA) on the ultrastructure and pigment composition of cyanobacterium Microcystis aeruginosa. | 2009-10 |
|
| Responses of enzymatic antioxidants and non-enzymatic antioxidants in the cyanobacterium Microcystis aeruginosa to the allelochemical ethyl 2-methyl acetoacetate (EMA) isolated from reed (Phragmites communis). | 2008-08-25 |
|
| [Effects of allelochemical EMA from reed on the production and release of cyanotoxins in Microcystis aeruginosa]. | 2007-09 |
|
| High production of (2s,3s)-3-hydroxy-2-methylbutanoate by immobilized plant cells of Marchantia polymorpha. | 2007-06 |
|
| Stereochemical consequences of threefold symmetry in asymmetric catalysis: distorting C3 Chiral 1,1,1-tris(oxazolinyl)ethanes ("trisox") in CuII Lewis acid catalysts. | 2007 |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 23:30:10 GMT 2025
by
admin
on
Mon Mar 31 23:30:10 GMT 2025
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| Record UNII |
NE9WOZ20JE
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| Record Status |
Validated (UNII)
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| Record Version |
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| Code System | Code | Type | Description | ||
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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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