Chemical Properties of 2-Chloroethyl (E)-2-methylbut-2-enoate

2-Chloroethyl (E)-2-methylbut-2-enoate

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InChI
InChI=1S/C7H11ClO2/c1-3-6(2)7(9)10-5-4-8/h3H,4-5H2,1-2H3/b6-3+
InChI Key
UTHIRZUMGCPHPR-ZZXKWVIFSA-N
Formula
C7H11ClO2
SMILES
CC=C(C)C(=O)OCCCl
Molecular Weight1
162.61
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Physical Properties

Property Value Unit Source
Δf -166.12 kJ/mol Joback Calculated Property
Δfgas -340.92 kJ/mol Joback Calculated Property
Δfus 19.76 kJ/mol Joback Calculated Property
Δvap 44.75 kJ/mol Joback Calculated Property
log10WS -1.62 Crippen Calculated Property
logPoct/wat 1.735 Crippen Calculated Property
McVol 124.870 ml/mol McGowan Calculated Property
Pc 3005.73 kPa Joback Calculated Property
Inp [1159.00; 1159.00]   Show Hide
Inp 1159.00 NIST
Inp 1159.00 NIST
Tboil 477.32 K Joback Calculated Property
Tc 672.15 K Joback Calculated Property
Tfus 251.69 K Joback Calculated Property
Vc 0.481 m3/kmol Joback Calculated Property

Temperature Dependent Properties

Property Value Unit Temperature (K) Source
Cp,gas [248.04; 303.98] J/mol×K [477.32; 672.15] Show Hide
Cp,gas 248.04 J/mol×K 477.32 Joback Calculated Property
Cp,gas 258.54 J/mol×K 509.79 Joback Calculated Property
Cp,gas 268.56 J/mol×K 542.26 Joback Calculated Property
Cp,gas 278.09 J/mol×K 574.74 Joback Calculated Property
Cp,gas 287.17 J/mol×K 607.21 Joback Calculated Property
Cp,gas 295.79 J/mol×K 639.68 Joback Calculated Property
Cp,gas 303.98 J/mol×K 672.15 Joback Calculated Property

Similar Compounds

2,2-Dichloroethyl (E)-2-methylbut-2-enoate. Ethyl tiglate. Ethyl trans-2-methyl-2-butenoate. 2-Butenoic acid, 2-methyl-, ethyl ester. (Z)-Ethyl 2-methylbut-2-enoate. 2-methyl-2-butenoic acid ethyl ester. 2,2,2-Trichloroethyl (E)-2-methylbut-2-enoate. 2-Propenoic acid, 2-methyl-, 2-chloroethyl ester. 2-Butenoic acid, 2-methyl-, 2-propenyl ester, (E)-. 2-Butenoic acid, 2-methyl-, propyl ester, (E)-. Propyl angelate. Butenyl tiglate, 3-methyl-2-. 3-methyl-2-butenyl 2-methylcrotonate. (E)-But-2-enyl (E)-2-methylbut-2-enoate. 2-Butenyl Angelate.

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

Sources

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