Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C5H10O |
| Molecular Weight | 86.1323 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CC(C)C(C)=O
InChI
InChIKey=SYBYTAAJFKOIEJ-UHFFFAOYSA-N
InChI=1S/C5H10O/c1-4(2)5(3)6/h4H,1-3H3
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Synthesis of ketonylplatinum(III) dinuclear complexes: observation of the competitive radical vs electrophilic displacement in Pt(III)-promoted C-H bond activation of ketones. | 2001 Jan 31 |
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| Time dependence in mixture toxicity with soft electrophiles: 1. Combined effects of selected SN2- and SNAr-reactive agents with a nonpolar narcotic. | 2007 Apr |
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| Asymmetric allylation of methyl ketones by using chiral phenyl carbinols. | 2009 Jun 15 |
|
| New 3H-indole synthesis by Fischer's method. Part I. | 2010 Apr 8 |
|
| Isolation and characterization of 4-tert-butylphenol-utilizing Sphingobium fuliginis strains from Phragmites australis rhizosphere sediment. | 2010 Oct |
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EPA PESTICIDE CODE |
44104
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11251
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9379
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V8DP6THY5O
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METHYL ISOPROPYL KETONE
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563-80-4
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7915
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209-264-3
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m7432
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DTXSID0022062
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SUBSTANCE RECORD
