Chemical Properties of cis-Hydroxymethylcyclopropane, 2-methyl-2-phenyl

cis-Hydroxymethylcyclopropane, 2-methyl-2-phenyl

InChI
InChI=1S/C11H14O/c1-11(7-10(11)8-12)9-5-3-2-4-6-9/h2-6,10,12H,7-8H2,1H3/t10-,11+/m1/s1
InChI Key
UHQXBASRPLGYEL-MNOVXSKESA-N
Formula
C11H14O
SMILES
CC1(c2ccccc2)CC1CO
Molecular Weight1
162.23
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Physical Properties

Property Value Unit Source
ω 0.5412 Relay (1.0) Calculated Property
ΔfG° 64.88 kJ/mol Joback Calculated Property
ΔfH°gas -67.97 kJ/mol Relay (1.0) Calculated Property
ΔfusH° 15.28 kJ/mol Joback Calculated Property
ΔvapH° 82.84 kJ/mol Relay (1.0) Calculated Property
IE 8.46 eV Relay (1.0) Calculated Property
log10WS -2.15 Relay (1.0) Calculated Property
logPoct/wat 1.956 Crippen Calculated Property
McVol 137.100 ml/mol McGowan Calculated Property
Pc 3423.86 kPa Joback Calculated Property
Inp 1295.00 NIST
Tboil 532.59 K Relay (1.0) Calculated Property
Tc 773.37 K Relay (1.0) Calculated Property
Tfus 301.25 K Relay (1.0) Calculated Property
Vc 0.471 m3/kmol Relay (1.0) Calculated Property

Temperature Dependent Properties

Property Value Unit Temperature (K) Source
Cp,gas [344.20; 416.09] J/mol×K [572.25; 783.32] Show Hide
Cp,gas 344.20 J/mol×K 572.25 Joback Calculated Property
Cp,gas 358.07 J/mol×K 607.43 Joback Calculated Property
Cp,gas 371.00 J/mol×K 642.61 Joback Calculated Property
Cp,gas 383.13 J/mol×K 677.78 Joback Calculated Property
Cp,gas 394.59 J/mol×K 712.96 Joback Calculated Property
Cp,gas 405.53 J/mol×K 748.14 Joback Calculated Property
Cp,gas 416.09 J/mol×K 783.32 Joback Calculated Property

Similar Compounds

trans-Hydroxymethylcyclopropane, 2-methyl-2-phenyl. cis-Methylcyclopropanecarboxylate, 2-methyl-2-phenyl. 1(Hydroxymethyl)-2,2-diphenylcyclopropane. Cyclopropane-1-carboxylic acid, 2-methoxymethyl-3-phenyl, ethyl ester. Milnacipran, N-trimethylsilyl-. Milnacipran. Milnacipran, N,N-bis(trimethylsilyl)-. 14-hydroxy-calamenene. 1-(Acetoxy methyl)-2,2-diphenyl cyclopropane. 15-Trimethylsilyloxydehydroabietic acid, trimethylsilyl ester. Cyclopropanecarboxylic acid, trans-2-phenyl-, cyclohexylmethyl ester. 1-Phenanthrenemethanol, 1,2,3,4,4a,9,10,10a-octahydro-1,4a-dimethyl-7-(1-methylethyl)-, [1R-(1«alpha»,4a«beta»,10a«alpha»)]-. Epidehydroabietol. 15-Hydroxy-7-oxodehydroabietic acid, trimethylsilyl ester, 15-trimethylsilyl ether. Cyclopropanecarboxylic acid, trans-2-phenyl-, 2-ethylhexyl ester.

Find more compounds similar to cis-Hydroxymethylcyclopropane, 2-methyl-2-phenyl.

Sources

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