CAS 3195-24-2
:Diethyl diallylmalonate
Description:
Diethyl diallylmalonate is an organic compound characterized by its structure, which includes two ethyl ester groups and two allyl groups attached to a malonate backbone. This compound typically appears as a colorless to pale yellow liquid with a fruity odor. It is soluble in organic solvents such as ethanol and ether but has limited solubility in water. Diethyl diallylmalonate is known for its reactivity, particularly in polymerization reactions, where it can serve as a monomer or crosslinking agent in the synthesis of various polymers. Additionally, it exhibits properties that make it useful in the production of specialty chemicals and as an intermediate in organic synthesis. Safety considerations should be taken into account when handling this compound, as it may pose risks such as skin and eye irritation. Overall, diethyl diallylmalonate is a versatile chemical with applications in both industrial and research settings.
Formula:C13H20O4
InChI:InChI=1S/C13H20O4/c1-5-9-13(10-6-2,11(14)16-7-3)12(15)17-8-4/h5-6H,1-2,7-10H2,3-4H3
InChI key:InChIKey=LYUUVYQGUMRKOV-UHFFFAOYSA-N
SMILES:C(C(OCC)=O)(C(OCC)=O)(CC=C)CC=C
Synonyms:- 2,2-(Diallyl)malonic acid diethyl ester
- Di-2-propenylpropanedioic acid diethyl ester
- Diethyl 2,2-diallylmalonate
- Diethyl Diprop-2-En-1-Ylpropanedioate
- Diethyl diallylmalonate
- Diethyl diallylpropanedioate
- Diethyl-2-allyl-2-butenylmalonate
- Malonic acid, diallyl-, diethyl ester
- NSC 30683
- NSC 46842
- Propanedioic acid, 2,2-di-2-propen-1-yl-, 1,3-diethyl ester
- See more synonyms
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Found 8 products.
Diethyl Diallylmalonate
CAS:Formula:C13H20O4Purity:>98.0%(GC)Color and Shape:Colorless to Almost colorless clear liquidMolecular weight:240.30Diethyl diallylmalonate, 97+%
CAS:<p>Diethyl diallylmalonate is the starting material for enantioselective synthesis of carbocyclic nucleoside analogues. It is also used as Low catalyst loading in ring-closing metathesis reaction. Cationic nickel (with monodentate phosphoramidites and Wilke?s azaphospholene as ligands) catalyzed cycloi</p>Formula:C13H20O4Purity:97+%Color and Shape:Liquid, Clear colorlessMolecular weight:240.30DIETHYL 2,2-DIALLYLMALONATE
CAS:Formula:C13H20O4Purity:98%Color and Shape:LiquidMolecular weight:240.2955diethyl 2,2-diallylmalonate
CAS:diethyl 2,2-diallylmalonateFormula:C13H20O4Purity:98%Color and Shape: colourless liquidMolecular weight:240.30g/molDiethyl Diallylmalonate
CAS:Formula:C13H20O4Purity:98% (stabilized with MEHQ)Color and Shape:LiquidMolecular weight:240.299Diethyl Diallylmalonate
CAS:Controlled ProductFormula:C13H20O4Color and Shape:NeatMolecular weight:240.3Diethyl Diallylmalonate
CAS:<p>Diethyl diallylmalonate is a hydroxyl-containing compound that can be used as a solid catalyst for the metathesis reaction. It has been shown to have high activity in catalyzing the formation of amides from carboxylic acids and amines, which is an important chemical reaction in organic synthesis. Furthermore, it can be regenerated by oxidation or reduction, making it an efficient catalyst. This product also has a high redox potential and can be activated by a variety of catalysts. Diethyl diallylmalonate is often used as a model system for fatty acid metathesis reactions.</p>Formula:C13H20O4Purity:Min. 95%Molecular weight:240.3 g/mol







