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Merck
CN

713309

Methyl 2-oxobutanoate

95%

Synonym(s):

2-Oxobutyric acid methyl ester, Methyl 2-ketobutyrate

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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
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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

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.

pictograms

FlameCorrosion

signalword

Danger

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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