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About This Item
Linear Formula:
C2H5OCOC(ONa)=CHCOOC2H5
CAS Number:
Molecular Weight:
210.16
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
255-122-9
Beilstein/REAXYS Number:
4279609
MDL number:
Assay:
95%
Quality Level
assay
95%
mp
188-190 °C (lit.)
functional group
ester
SMILES string
[Na+].CCOC(=O)\C=C(/[O-])C(=O)OCC
InChI
1S/C8H12O5.Na/c1-3-12-7(10)5-6(9)8(11)13-4-2;/h5,9H,3-4H2,1-2H3;/q;+1/p-1/b6-5-;
InChI key
UJZUICGIJODKOS-YSMBQZINSA-M
Application
Diethyl oxalacetate sodium salt can be used as a reagent to synthesize:
- Spiro[indoline-3,4′-pyrano[2,3-c]pyrazole derivatives via a one-pot reaction with isatins, malononitrile, and hydrazine hydrate.
- 2,3-dioxo-4-carboxy-5-substituted pyrrolidines by reacting with various aldehydes and primary amines.
- 2-nitro-4-fluoro triazole diester by treating with 2-nitro-4-fluoro-phenylazide.
signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
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Diethyl oxalacetate sodium salt as a reagent to obtain functionalized spiro [indoline-3, 4?-pyrano [2, 3-c] pyrazoles]
Gein VL, et al.
Tetrahedron Letters, 58(2), 134-136 (2017)
Synthesis of novel 3, 4-fused pyrazolidinone ?-lactam bicyclic moieties from 2, 3-dioxo-4-carboxy-5-(substituted) pyrrolidines
Rashid FNAA, et al.
Organic Communications, 12(3), 121-131 (2019)
PYRUVATE CARBOXYLASE. I. NATURE OF THE REACTION.
M F UTTER et al.
The Journal of biological chemistry, 238, 2603-2608 (1963-08-01)
Global Trade Item Number
| SKU | GTIN |
|---|---|
| 171263-500G | 04061831828689 |
| 171263-100G | 04061838750822 |
