Chemical Properties of 2-Hydroxy-3-methoxycarbonyl-pentanedioic acid dimethyl ester

2-Hydroxy-3-methoxycarbonyl-pentanedioic acid dimethyl ester

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InChI Key
Molecular Weight1

Physical Properties

Property Value Unit Source
Δf -698.06 kJ/mol Joback Calculated Property
Δfgas -993.06 kJ/mol Joback Calculated Property
Δfus 20.28 kJ/mol Joback Calculated Property
Δvap 70.03 kJ/mol Joback Calculated Property
logPoct/wat -0.90 Crippen Calculated Property
Pc 3076.16 kPa Joback Calculated Property
Tboil 648.74 K Joback Calculated Property
Tc 830.16 K Joback Calculated Property
Tfus 377.29 K Joback Calculated Property
Vc 0.56 m3/kg-mol Joback Calculated Property

Temperature Dependent Properties

Property Value Unit Temperature (K) Source
Cp,gas 397.46 J/mol×K 648.74 Joback Calculated Property
η 0.00 Pa×s 648.74 Joback Calculated Property

Molecular Descriptors

Joback and Reid Groups
>CH- 2
-O- (nonring) 3
>C=O (nonring) 2
-OH (alcohol) 1
-CH2- 1
-CH3 3

Similar Compounds

3,4-Dimethoxy adipic acid, dimethyl ester. Ribonic acid, 1,4-lactone, TMS. D-(+)-Ribonic acid «gamma»-lactone. 2-Hydroxyglutaric acid diethyl ester. d-Gluconic acid, 2,3,4,6-tetra-O-methyl-, «delta»-lactone. D-Gluconic acid, «delta»-lactone. Gluconic acid «delta»-lactone. Butanedioic acid, methoxy-, dimethyl ester. D-(+)-Ribono-1,4-lactone, triacetate. Butanedioic acid, 2,3-dihydroxy- [R-(R*,R*)]-, dimethyl ester. dimethyl [S(R*,R*)]-tartrate. DL-Dimethyl tartarate. Meso-tartaric acid, dimethylester. D-glucaro-3,6-lactone. D-(tetrahydro-2,3,4-trihydroxy-5-oxofuran-2-yl)glycollic acid.

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