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pd_meltingpoint:-13°C(lit.)
Appearance:COA
Purity:99%
Synthesis Reference(s) |
Organic Syntheses, Coll. Vol. 4, p. 417, 1963Tetrahedron Letters, 26, p. 1411, 1985 DOI: 10.1016/S0040-4039(00)99058-0 |
InChI:InChI=1/C5H8O4/c1-2-9-5(8)3-4(6)7/h2-3H2,1H3,(H,6,7)
A simple and efficient electrocarboxylat...
The process development of ethyl-(R)-3-a...
2-Alkyloxaziridine-3,3-dicarboxylic acid...
A new stereoselective alkylation methodo...
The highly efficient selective monohydro...
-
Starting from both the bridging nitrogen...
A practical large-scale synthesis of mon...
Boric acid catalyzes the monoesterificat...
Malonic anhydrides decompose at or below...
-
Enantioenriched acyclic α-substituted β-...
A thirteen-step total synthesis of (±)-s...
The present disclosure relates to antiba...
We present an effective deacylative alky...
ethyl malonamate
acetamide
malonic acid
hydrogen ethyl malonate
acetic acid
Conditions | Yield |
---|---|
With
phthalic anhydride;
at 240 - 250 ℃;
for 1h;
under 3040 Torr;
|
53% |
3,4-dibromo-2-oxo-but-3-ene-1,1,4-tricarboxylic acid-1,1-diethyl ester
dibromomaleic acid
hydrogen ethyl malonate
Conditions | Yield |
---|---|
Erwaermen;
|
ethanol
malonic acid
ethyl acetate
diethyl malonate
(2E,4E)-ethyl hexa-2,4-dienoate
ethyl (E)-3-(benzo[d][1,3]dioxol-5-yl)acrylate
ethyl (2E)-non-2-enoate
ethyl 2-heptenoate
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