165263
2-乙基乙酰乙酸乙酯
90%
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关于此项目
线性分子式:
CH3COCH(C2H5)COOC2H5
化学文摘社编号:
分子量:
158.19
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
210-151-6
Beilstein/REAXYS Number:
636286
MDL number:
Assay:
90%
Form:
liquid
InChI key
OKANYBNORCUPKZ-UHFFFAOYSA-N
InChI
1S/C8H14O3/c1-4-7(6(3)9)8(10)11-5-2/h7H,4-5H2,1-3H3
SMILES string
CCOC(=O)C(CC)C(C)=O
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.)
functional group
ester, ketone
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.
存储类别
10 - Combustible liquids
wgk
WGK 1
flash_point_f
156.2 °F - closed cup
flash_point_c
69 °C - closed cup
ppe
Eyeshields, Gloves, multi-purpose combination respirator cartridge (US)
法规信息
新产品
此项目有
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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