Chemical Properties of Diallyl malonate

Diallyl malonate

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InChI
InChI=1S/C9H12O4/c1-3-5-12-8(10)7-9(11)13-6-4-2/h3-4H,1-2,5-7H2
InChI Key
AOESAXAWXYJFNC-UHFFFAOYSA-N
Formula
C9H12O4
SMILES
C=CCOC(=O)CC(=O)OCC=C
Molecular Weight1
184.19
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Physical Properties

Property Value Unit Source
Δf -267.26 kJ/mol Joback Calculated Property
Δfgas -467.83 kJ/mol Joback Calculated Property
Δfus 22.08 kJ/mol Joback Calculated Property
Δvap 52.60 kJ/mol Joback Calculated Property
log10WS -1.02 Crippen Calculated Property
logPoct/wat 0.835 Crippen Calculated Property
McVol 143.950 ml/mol McGowan Calculated Property
Pc 2752.67 kPa Joback Calculated Property
Inp 1178.00 NIST
Tboil 551.26 K Joback Calculated Property
Tc 739.86 K Joback Calculated Property
Tfus 331.99 K Joback Calculated Property
Vc 0.549 m3/kmol Joback Calculated Property

Temperature Dependent Properties

Property Value Unit Temperature (K) Source
Cp,gas [329.13; 388.46] J/mol×K [551.26; 739.86] Show Hide
Cp,gas 329.13 J/mol×K 551.26 Joback Calculated Property
Cp,gas 340.24 J/mol×K 582.69 Joback Calculated Property
Cp,gas 350.85 J/mol×K 614.13 Joback Calculated Property
Cp,gas 360.99 J/mol×K 645.56 Joback Calculated Property
Cp,gas 370.63 J/mol×K 676.99 Joback Calculated Property
Cp,gas 379.79 J/mol×K 708.42 Joback Calculated Property
Cp,gas 388.46 J/mol×K 739.86 Joback Calculated Property
η [0.0002211; 0.0018303] Pa×s [331.99; 551.26] Show Hide
η 0.0018303 Pa×s 331.99 Joback Calculated Property
η 0.0010807 Pa×s 368.54 Joback Calculated Property
η 0.0007017 Pa×s 405.08 Joback Calculated Property
η 0.0004894 Pa×s 441.62 Joback Calculated Property
η 0.0003606 Pa×s 478.17 Joback Calculated Property
η 0.0002775 Pa×s 514.71 Joback Calculated Property
η 0.0002211 Pa×s 551.26 Joback Calculated Property

Similar Compounds

Propanoic acid, 2-propenyl ester. Butanoic acid, 3-oxo-, 2-propenyl ester. Propanoic acid, 3-chloro, 2-propenyl ester. Diallyl succinate. Diethyl malonate. Allyl acetate. Malonic acid, di(2,2-dichloroethyl) ester. Propanoic acid, 2-methyl-, 2-propenyl ester. Butanoic acid, 2-propenyl ester. Allyl bromoacetate. Chloroacetic acid allyl ester. 2-Buten-1-ol, propanoate. Allyl isovalerate. Propanoic acid, 2-chloro-, 2-propenyl ester. Malonic acid, 2,2-dichloroethyl ethyl ester.

Find more compounds similar to Diallyl malonate.

Sources

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