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About This Item
Empirical Formula (Hill Notation):
C5H8O3
CAS Number:
Molecular Weight:
116.12
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
1749847
Assay:
≥95.0% (GC), 95%
Form:
liquid
InChI key
XPIWVCAMONZQCP-UHFFFAOYSA-N
SMILES string
CCC(=O)C(=O)OC
InChI
1S/C5H8O3/c1-3-4(6)5(7)8-2/h3H2,1-2H3
assay
≥95.0% (GC), 95%
form
liquid
impurities
≤1.0% water
functional group
ester, ketone
Quality Level
Related Categories
Application
Methyl 2-oxobutanoate can be used as a starting material:
- To synthesize indole derivatives via Fischer indolization of arylhydrazines using propylphosphonic anhydride.
- In the synthesis of (−)-picrotoxinin, a natural product and neurotoxic sesquiterpenoid.
- To prepare the core structure of phalarine, a natural product found in perennial grass.
signalword
Danger
hcodes
Hazard Classifications
Eye Dam. 1 - Flam. Liq. 3 - Skin Irrit. 2
Storage Class
3 - Flammable liquids
wgk
WGK 2
flash_point_f
122.0 °F
flash_point_c
50 °C
ppe
Eyeshields, Gloves, type ABEK (EN14387) respirator filter
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Synthesis of the core structure of phalarine
Douki K, et al.
Organic & Biomolecular Chemistry, 17, 1727-1730 (2019)
A microwave-assisted, propylphosphonic anhydride (T3P) mediated one-pot Fischer indole synthesis
Desroses M, et al.
Tetrahedron Letters, 52, 4417-4420 (2011)
Synthesis of (−)-Picrotoxinin by Late-Stage Strong Bond Activation
Crossley SWM, et al.
Journal of the American Chemical Society, 142, 11376-11381 (2020)
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