Chemical Properties of 2-Methyl-2-propenoic acid (CAS 816-74-0)

2-Methyl-2-propenoic acid

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InChI
InChI=1S/C8H12O2/c1-6(2)5-10-8(9)7(3)4/h1,3,5H2,2,4H3
InChI Key
TVBLIEXOPWWREN-UHFFFAOYSA-N
Formula
C8H12O2
SMILES
C=C(C)COC(=O)C(=C)C
Molecular Weight1
140.18
CAS
816-74-0
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Physical Properties

Property Value Unit Source
Δf -58.86 kJ/mol Joback Calculated Property
Δfgas -221.97 kJ/mol Joback Calculated Property
Δfus 14.08 kJ/mol Joback Calculated Property
Δvap 41.38 kJ/mol Joback Calculated Property
log10WS -1.74 Crippen Calculated Property
logPoct/wat 1.682 Crippen Calculated Property
McVol 122.420 ml/mol McGowan Calculated Property
Pc 2934.52 kPa Joback Calculated Property
Inp [954.00; 954.00]   Show Hide
Inp 954.00 NIST
Inp 954.00 NIST
Tboil 451.85 K Joback Calculated Property
Tc 641.06 K Joback Calculated Property
Tfus 220.64 K Joback Calculated Property
Vc 0.471 m3/kmol Joback Calculated Property

Temperature Dependent Properties

Property Value Unit Temperature (K) Source
Cp,gas [246.48; 307.49] J/mol×K [451.85; 641.06] Show Hide
Cp,gas 246.48 J/mol×K 451.85 Joback Calculated Property
Cp,gas 257.84 J/mol×K 483.38 Joback Calculated Property
Cp,gas 268.71 J/mol×K 514.92 Joback Calculated Property
Cp,gas 279.10 J/mol×K 546.45 Joback Calculated Property
Cp,gas 289.02 J/mol×K 577.99 Joback Calculated Property
Cp,gas 298.48 J/mol×K 609.52 Joback Calculated Property
Cp,gas 307.49 J/mol×K 641.06 Joback Calculated Property

Similar Compounds

2-methylallyl 2-methylcrotonate. Methallyl angelate. (E)-2-Methylbut-2-en-1-yl methacrylate. 2-Propenoic acid, 2-methyl-, 2-propenyl ester. 2-Propenoic acid, 2-methyl-, propyl ester. (Z)-(E)-2-Methylbut-2-en-1-yl 2-methylbut-2-enoate. Angelyl Angelate. 2-Propen-1-ol, 2-methyl-, acetate. Dimethallyl ether. Methacrylic acid, ethyl ester. 2-Propenoic acid, 2-methyl-, 2-methylpropyl ester. 2-methylallyl isobutyrate. Methacrylic acid, 2,2,2-trichloroethyl ester. 2,2,2-Trifluoroethyl methacrylate. Methacrylic acid, 2-hydroxyethyl ester.

Find more compounds similar to 2-Methyl-2-propenoic acid.

Sources

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