67260
5-Methyl-3-heptanone
≥94% (GC)
Synonym(s):
Ethyl isoamyl ketone
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About This Item
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Assay
≥94% (GC)
refractive index
n20/D 1.414 (lit.)
bp
157-162 °C (lit.)
density
0.823 g/mL at 25 °C (lit.)
functional group
ketone
SMILES string
CCC(C)CC(=O)CC
InChI
1S/C8H16O/c1-4-7(3)6-8(9)5-2/h7H,4-6H2,1-3H3
InChI key
PSBKJPTZCVYXSD-UHFFFAOYSA-N
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Application
- 5-Methyl-3-heptanone can be converted into the corresponding gem-dihydroperoxide using aqueous hydrogen peroxide and chlorosulfonic acid as a catalyst at room temperature.
- It can be reduced to its corresponding alcohol using sodium borohydride in urea/choline chloride eutectic salt.
- It can undergo condensation with tert-butyl-sulfinamide to form the corresponding chiral tert-butyl-sulfinyl-ketimine, which can further react with ylides derived from trimethylsulfonium iodide and S-allyl tetrahydrothiophenium bromide to form highly substituted chiral aziridines.
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye Irrit. 2 - Flam. Liq. 3 - STOT SE 3
Target Organs
Respiratory system
Storage Class Code
3 - Flammable liquids
WGK
WGK 1
Flash Point(F)
111.2 °F - closed cup
Flash Point(C)
44 °C - closed cup
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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An efficient synthesis of gem-dihydroperoxides and 1, 2, 4, 5-tetraoxanes catalyzed bychlorosulfonic acid as a new catalyst.?
JOURNAL OF ADVANCES IN CHEMISTRY, 11(3), 3381-3390 (2015)
Natural deep eutectic salt promoted regioselective reduction of epoxides and carbonyl compounds.
Royal Society of Chemistry Advances, 2(6), 2289-2293 (2012)
Direct synthesis of chiral aziridines from N-tert-butyl-sulfinylketimines.
Chemical Communications (Cambridge, England), (17), 1833-1835 (2006)
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