Chemical Properties of sec-Butyl (E)-2-methylbut-2-enoate

sec-Butyl (E)-2-methylbut-2-enoate

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InChI
InChI=1S/C9H16O2/c1-5-7(3)9(10)11-8(4)6-2/h5,8H,6H2,1-4H3/b7-5+
InChI Key
UKJTZSWULQNVJI-FNORWQNLSA-N
Formula
C9H16O2
SMILES
CC=C(C)C(=O)OC(C)CC
Molecular Weight1
156.22
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Physical Properties

Property Value Unit Source
Δf -139.79 kJ/mol Joback Calculated Property
Δfgas -371.74 kJ/mol Joback Calculated Property
Δfus 17.22 kJ/mol Joback Calculated Property
Δvap 44.43 kJ/mol Joback Calculated Property
log10WS -2.42 Crippen Calculated Property
logPoct/wat 2.294 Crippen Calculated Property
McVol 140.810 ml/mol McGowan Calculated Property
Pc 2574.11 kPa Joback Calculated Property
Inp 1068.00 NIST
Tboil 485.21 K Joback Calculated Property
Tc 674.06 K Joback Calculated Property
Tfus 229.31 K Joback Calculated Property
Vc 0.538 m3/kmol Joback Calculated Property

Temperature Dependent Properties

Property Value Unit Temperature (K) Source
Cp,gas [306.09; 378.31] J/mol×K [485.21; 674.06] Show Hide
Cp,gas 306.09 J/mol×K 485.21 Joback Calculated Property
Cp,gas 319.56 J/mol×K 516.68 Joback Calculated Property
Cp,gas 332.44 J/mol×K 548.16 Joback Calculated Property
Cp,gas 344.74 J/mol×K 579.63 Joback Calculated Property
Cp,gas 356.48 J/mol×K 611.11 Joback Calculated Property
Cp,gas 367.66 J/mol×K 642.58 Joback Calculated Property
Cp,gas 378.31 J/mol×K 674.06 Joback Calculated Property

Similar Compounds

Pentan-2-yl (E)-2-methylbut-2-enoate. Pentan-2-yl 2-methylbut-2-enoate. 3-Methylbutan-2-yl (E)-2-methylbut-2-enoate. Hexan-3-yl (E)-2-methylbut-2-enoate. Hexan-2-yl (E)-2-methylbut-2-enoate. Octan-2-yl (E)-2-methylbut-2-enoate. Decan-2-yl (E)-2-methylbut-2-enoate. 3,3-Dimethylbutan-2-yl (E)-2-methylbut-2-enoate. Sec-butylcrotonate. 2-Butenoic acid, 1-methylpropyl ester, (E)-. 3-Oxobutan-2-yl (E)-2-methylbut-2-enoate. 4-Methylpentan-2-yl (E)-2-methylbut-2-enoate. 2,4-Dimethylpentan-3-yl (E)-2-methylbut-2-enoate. Isopropyl tiglate. 2-Butenoic acid, 2-methyl-, butyl ester, (Z)-.

Find more compounds similar to sec-Butyl (E)-2-methylbut-2-enoate.

Sources

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