Chemical Properties of Thymyl formate

Thymyl formate

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InChI
InChI=1S/C11H14O2/c1-8(2)10-5-4-9(3)6-11(10)13-7-12/h4-8H,1-3H3
InChI Key
IWAIRWGSZFYSES-UHFFFAOYSA-N
Formula
C11H14O2
SMILES
Cc1ccc(C(C)C)c(OC=O)c1
Molecular Weight1
178.23
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Physical Properties

Property Value Unit Source
ω 0.5469 Relay (... Calculated Property
Δf -72.07 kJ/mol Joback Calculated Property
Δfgas -321.03 kJ/mol Relay (... Calculated Property
Δfus 17.46 kJ/mol Joback Calculated Property
Δvap 63.56 kJ/mol Relay (... Calculated Property
IE 8.30 eV Relay (... Calculated Property
log10WS -3.30 Relay (... Calculated Property
logPoct/wat 2.654 Crippen Calculated Property
McVol 149.530 ml/mol McGowan Calculated Property
Pc 2746.90 kPa Joback Calculated Property
Inp 1262.00 NIST
Tboil 512.01 K Relay (... Calculated Property
Tc 717.77 K Relay (... Calculated Property
Tfus 294.09 K Relay (... Calculated Property
Vc 0.530 m3/kmol Relay (... Calculated Property

Temperature Dependent Properties

Property Value Unit Temperature (K) Source
Cp,gas [347.05; 419.80] J/mol×K [558.36; 769.26] Show Hide
Cp,gas 347.05 J/mol×K 558.36 Joback Calculated Property
Cp,gas 360.93 J/mol×K 593.51 Joback Calculated Property
Cp,gas 374.09 J/mol×K 628.66 Joback Calculated Property
Cp,gas 386.55 J/mol×K 663.81 Joback Calculated Property
Cp,gas 398.32 J/mol×K 698.96 Joback Calculated Property
Cp,gas 409.40 J/mol×K 734.11 Joback Calculated Property
Cp,gas 419.80 J/mol×K 769.26 Joback Calculated Property
η [0.0001956; 0.0018829] Pa×s [314.42; 558.36] Show Hide
η 0.0018829 Pa×s 314.42 Joback Calculated Property
η 0.0010402 Pa×s 355.08 Joback Calculated Property
η 0.0006491 Pa×s 395.73 Joback Calculated Property
η 0.0004423 Pa×s 436.39 Joback Calculated Property
η 0.0003217 Pa×s 477.05 Joback Calculated Property
η 0.0002460 Pa×s 517.70 Joback Calculated Property
η 0.0001956 Pa×s 558.36 Joback Calculated Property

Similar Compounds

Benzene, 2-methoxy-4-methyl-1-(1-methylethyl)-. Phenol, 5-methyl-2-(1-methylethyl)-, acetate. Formic acid, 2-isopropylphenyl ester. Thymyl methacrylate. Thymyl isobutyrate. 2,5-Dimethoxy-p-cymene. Carvacrol methyl ether. o-Isopropylanisole. Thymyl tiglate. Thymyl angelate. Benzene, 1-(1,1-dimethylethyl)-2-methoxy-4-methyl-. Benzene, 1-methoxy-4-methyl-2-(1-methylethyl)-. Carvacrol, ethyl ether. Phenol, 2-methyl-5-(1-methylethyl)-, acetate. Phenol, 2-methyl-5-(1-methylethyl)-, acetate.

Find more compounds similar to Thymyl formate.

Sources

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