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线性分子式:
(C2H5)2C(COOH)2
化学文摘社编号:
分子量:
160.17
UNSPSC Code:
12162002
NACRES:
NA.23
PubChem Substance ID:
EC Number:
208-111-8
Beilstein/REAXYS Number:
1768554
MDL number:
InChI key
LTMRRSWNXVJMBA-UHFFFAOYSA-N
InChI
1S/C7H12O4/c1-3-7(4-2,5(8)9)6(10)11/h3-4H2,1-2H3,(H,8,9)(H,10,11)
SMILES string
CCC(CC)(C(O)=O)C(O)=O
assay
98%
form
powder
mp
129-131 °C (lit.)
Quality Level
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
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
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
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
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)
Y Suhara et al.
Bioorganic & medicinal chemistry letters, 11(15), 1985-1988 (2001-07-17)
Novel analogues of 2-arachidonoylglycerol (2-AG), an endogenous cannabinoid receptor ligand, were developed. Chemical synthesis of these analogues (2-AGA105 and 2-AGA109) was accomplished starting from 2-octyn-1-ol and diethyl malonate and employing Wittig coupling of triene phosphonate with an aldehyde intermediate in
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