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About This Item
Linear Formula:
CH3COCH(C2H5)COOC2H5
CAS Number:
Molecular Weight:
158.19
Beilstein:
636286
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
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Assay
90%
form
liquid
refractive index
n20/D 1.421 (lit.)
bp
87-189 °C/743 mmHg (lit.)
density
0.981 g/mL at 25 °C (lit.)
SMILES string
CCOC(=O)C(CC)C(C)=O
InChI
1S/C8H14O3/c1-4-7(6(3)9)8(10)11-5-2/h7H,4-5H2,1-3H3
InChI key
OKANYBNORCUPKZ-UHFFFAOYSA-N
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Application
Ethyl 2-ethylacetoacetate was used in the synthesis of 2-alkylidenetetrahydrofurans, diphenyllead(IV) thiosemicarbazonates and pyrazolonates. It was used as starting reagent in the synthesis of 2-ethylfumaric acid.
Storage Class Code
10 - Combustible liquids
WGK
WGK 1
Flash Point(F)
156.2 °F - closed cup
Flash Point(C)
69 °C - closed cup
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Certificates of Analysis (COA)
Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.
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Diphenyllead (IV) thiosemicarbazonates and pyrazolonates: Synthesis and characterization.
Casas JS, et al.
Polyhedron, 28(5), 1029-1039 (2009)
Hans Raj et al.
Applied microbiology and biotechnology, 94(2), 385-397 (2011-10-19)
Methylaspartate ammonia lyase (MAL; EC 4.3.1.2) catalyzes the reversible addition of ammonia to mesaconate to give (2S,3S)-3-methylaspartate and (2S,3R)-3-methylaspartate as products. MAL is of considerable biocatalytic interest because of its potential use for the asymmetric synthesis of substituted aspartic acids
Efficient synthesis of functionalized furans and benzofurans based on a '[3+ 2] cyclization/oxidation'strategy.
Bellur E, et al.
Tetrahedron Letters, 46(13), 2185-2187 (2005)
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