Chemical Properties of Dimethyl methoxymalonate (CAS 5018-30-4)

Dimethyl methoxymalonate

InChI
InChI=1S/C6H10O5/c1-9-4(5(7)10-2)6(8)11-3/h4H,1-3H3
InChI Key
ORXJMBXYSGGCHG-UHFFFAOYSA-N
Formula
C6H10O5
SMILES
COC(=O)C(OC)C(=O)OC
Molecular Weight1
162.14
CAS
5018-30-4
Other Names
  • Methoxymalonic acid dimethyl ester
  • Propanedioic acid, methoxy-, dimethyl ester
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Physical Properties

Property Value Unit Source
ω 0.5167 Relay (1.0) Calculated Property
Δf -575.64 kJ/mol Joback Calculated Property
Δfgas -886.71 kJ/mol Relay (1.0) Calculated Property
Δfus 14.54 kJ/mol Joback Calculated Property
Δvap 63.94 kJ/mol Relay (1.0) Calculated Property
IE 9.57 eV Relay (1.0) Calculated Property
log10WS 0.17 Relay (1.0) Calculated Property
logPoct/wat -0.653 Crippen Calculated Property
McVol 116.150 ml/mol McGowan Calculated Property
Pc 3415.86 kPa Joback Calculated Property
Tboil 467.08 K Relay (1.0) Calculated Property
Tc 637.69 K Relay (1.0) Calculated Property
Tfus 277.69 K Relay (1.0) Calculated Property
Vc 0.423 m3/kmol Relay (1.0) Calculated Property

Temperature Dependent Properties

Property Value Unit Temperature (K) Source
Cp,gas [258.28; 310.89] J/mol×K [511.24; 701.91] Show Hide
Cp,gas 258.28 J/mol×K 511.24 Joback Calculated Property
Cp,gas 267.81 J/mol×K 543.02 Joback Calculated Property
Cp,gas 277.07 J/mol×K 574.80 Joback Calculated Property
Cp,gas 286.03 J/mol×K 606.57 Joback Calculated Property
Cp,gas 294.67 J/mol×K 638.35 Joback Calculated Property
Cp,gas 302.96 J/mol×K 670.13 Joback Calculated Property
Cp,gas 310.89 J/mol×K 701.91 Joback Calculated Property
η [0.0002085; 0.0020172] Pa×s [308.93; 511.24] Show Hide
η 0.0020172 Pa×s 308.93 Joback Calculated Property
η 0.0011472 Pa×s 342.65 Joback Calculated Property
η 0.0007218 Pa×s 376.37 Joback Calculated Property
η 0.0004902 Pa×s 410.09 Joback Calculated Property
η 0.0003530 Pa×s 443.80 Joback Calculated Property
η 0.0002663 Pa×s 477.52 Joback Calculated Property
η 0.0002085 Pa×s 511.24 Joback Calculated Property

Similar Compounds

Tartronic acid, diethyl ester, acetate. Methyl 2,3-dimethoxy-3-butenoate. 2,3-Diethoxy-propionic acid, ethyl ester. Butanedioic acid, methoxy-, dimethyl ester. DL-Glyceraldehyde, dimethyl ether. Propanedioic acid, dimethyl ester. Ethyl 2-ethoxypropanoate. ethyl 2-acetoxypropanoate. Propanedioic acid, bromo-, dimethyl ester. Propane, 1,2,3-trimethoxy-. Dimethyl chloromalonate. 1,4-Dioxane-2,5-dione, 3,6-dimethyl-. DL-Lactide. 1,4-Dioxane-2,5-dione, 3,6-dimethyl-, (3S-cis)-. Methyl «alpha»,«beta»-isopropylidene-D-glycerate.

Find more compounds similar to Dimethyl methoxymalonate.

Sources

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