All Photos(1)
About This Item
Linear Formula:
(C2H5)2C(COOH)2
CAS Number:
Molecular Weight:
160.17
Beilstein:
1768554
EC Number:
MDL number:
UNSPSC Code:
12162002
PubChem Substance ID:
NACRES:
NA.23
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Quality Level
Assay
98%
form
powder
mp
129-131 °C (lit.)
SMILES string
CCC(CC)(C(O)=O)C(O)=O
InChI
1S/C7H12O4/c1-3-7(4-2,5(8)9)6(10)11/h3-4H2,1-2H3,(H,8,9)(H,10,11)
InChI key
LTMRRSWNXVJMBA-UHFFFAOYSA-N
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Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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W G Reifenrath et al.
Journal of pharmaceutical sciences, 73(10), 1388-1392 (1984-10-01)
A shower decontamination bench model has been used to assess quantitatively the importance of several variables (water pressure and temperature, surfactant concentration in the decontamination fluid, nozzle type, and shower time) on decontamination of nontoxic chemical warfare-agent simulants diethyl malonate
Effects of diethylmalonate & alpha-picolinic acid on levels of inorganic nitrogen & tricarboxylic acid cycle enzymes in L-alanine utilizing B. brevis.
R P Singh et al.
Indian journal of biochemistry & biophysics, 20(1), 39-42 (1983-02-01)
Hong-Min Liu et al.
Carbohydrate research, 338(17), 1737-1743 (2003-08-02)
A butenolide-containing sugar available from the aldol condensation of methyl 4,6-O-benzylidene-alpha-D-glucopyranosid-2-ulose with diethyl malonate is autoxidized at the C-3 position into the corresponding alpha,beta-unsaturated gamma-lactone sugar by air, which subsequently undergoes 1,4-conjugate (Michael) addition of hydroxide ion (or water) leading
M A Hassan
Journal of hazardous materials, 88(1), 33-49 (2001-10-19)
Three malonanilide dimers (MA2-MA4) were prepared by the reaction of ethyl malonate with malonanilide derivatives (M2-M4). These dimers were investigated as new stabilizers for nitrocellulose. The evaluation process has been performed through Bergman-Junk (BJ) test, thermal analysis measurements (TGA and
D Matosiuk et al.
Acta poloniae pharmaceutica, 53(3), 209-212 (1996-05-01)
Cyclocondensation of 1,5-disubstituted 2-aminoimidazolines with diethyl malonate in the presence of sodium methanolate leading to imidazol[1,2-alpyrimidine-5,7-dion system is presented. Prevailing of 7-hydroxy-5(1H)oxo form between three possible tautomers is discussed based on spectral data. CNS activity of nine compounds is evaluated.
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