Chemical Properties of 2,3-Epoxypropyl-p-methoxyphenylether

2,3-Epoxypropyl-p-methoxyphenylether

InChI
InChI=1S/C10H12O3/c1-11-8-2-4-9(5-3-8)12-6-10-7-13-10/h2-5,10H,6-7H2,1H3
InChI Key
AVWGFHZLPMLKBL-UHFFFAOYSA-N
Formula
C10H12O3
SMILES
COc1ccc(OCC2CO2)cc1
Molecular Weight1
180.20
Other Names
  • ((4-Methoxyphenoxy)methyl)oxirane
  • 1,2-Epoxy-3-(p-methoxyphenoxy)propane
  • 1-(4-Methoxyphenoxy)-2,3-epoxypropane
  • 1-(p-Methoxyphenoxy)-2,3-epoxypropane
  • 2,3-Epoxypropyl p-methoxyphenyl ether
  • 2,3-Epoxypropyl para-methoxyphenyl ether
  • 2,3-Epoxypropyl-4-methoxyphenyl ether
  • 2,3-epoxypropyl 4'-methoxyphenyl ether
  • 2-(p-Methoxyphenoxymethyl)oxirane
  • 3-(4-Methoxyphenoxy)-1,2-epoxypropane
  • Anisole, p-(2,3-epoxypropoxy)-
  • Benzene, 1-(2,3-epoxypropoxy)-4-methoxy-
  • Glycidyl 4-methoxyphenyl ether
  • Glycidyl p-methoxyphenyl ether
  • Methoxyphenyl glycidyl ether
  • NSC 126709
  • NSC 26796
  • Oxirane, [(4-methoxyphenoxy)methyl]-
  • p-Methoxyphenyl glycidyl ether
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Physical Properties

Property Value Unit Source
ΔfH°gas -276.21 kJ/mol Relay (1.0) Calculated Property
ΔfusH° 23.80 kJ/mol Joback Calculated Property
ΔvapH° 78.59 kJ/mol Relay (1.0) Calculated Property
IE 8.29 eV Relay (1.0) Calculated Property
logPoct/wat 1.473 Crippen Calculated Property
McVol 134.750 ml/mol McGowan Calculated Property
Pc 3173.97 kPa Joback Calculated Property
Tboil 569.04 K Relay (1.0) Calculated Property
Tc 757.18 K Relay (1.0) Calculated Property
Tfus 320.15 K Jean-Claude Bradley Open Melting Point Dataset (2014, CC0) Compiled value

Cheméo can also estimate Critical Volume, Standard Gibbs free energy of formation, Acentric Factor, Log10 of Water solubility in mol/l for this compound, but they fall outside the models' validated range, so they are not shown here. Open the prediction tool to compute them on demand.

Correlations

Property Value Unit Temperature (K) Source
Cp,gas [187.64; 449.93] J/mol×K [273.00; 1000.00] Joback Predicted correlation Show Hide
EquationY = A + B·T + C·T² + D·T³ + E·T⁴
Y is Cp,gas in J/mol×K, T in K
Coefficient A-7.72900e+00
Coefficient B8.36920e-01
Coefficient C-4.68660e-04
Coefficient D8.94000e-08
Coefficient E0.00000e+00
Temperature range, min.273.00
Temperature range, max.1000.00
Cp,gas 187.64 J/mol×K 273.00 Calculated Property
Cp,gas 233.66 J/mol×K 353.78 Calculated Property
Cp,gas 274.79 J/mol×K 434.56 Calculated Property
Cp,gas 311.34 J/mol×K 515.33 Calculated Property
Cp,gas 343.57 J/mol×K 596.11 Calculated Property
Cp,gas 371.77 J/mol×K 676.89 Calculated Property
Cp,gas 396.22 J/mol×K 757.67 Calculated Property
Cp,gas 417.21 J/mol×K 838.44 Calculated Property
Cp,gas 435.02 J/mol×K 919.22 Calculated Property
Cp,gas 449.93 J/mol×K 1000.00 Calculated Property
Property Value Unit Temperature (K) Source
η [0.0015543; 0.0003587] Pa×s [320.15; 528.92] Joback Predicted correlation Show Hide
EquationY = exp(A + B/T + C·ln(T) + D·T^E)
Y is η in Pa×s, T in K
Coefficient A-1.01819e+01
Coefficient B1.18941e+03
Coefficient C0.00000e+00
Coefficient D0.00000e+00
Coefficient E0.00000e+00
CommentLiquid phase. Joback/Reid (1987), valid from Tf to 0.7·Tc.
Temperature range, min.320.15
Temperature range, max.528.92
η 0.0015543 Pa×s 320.15 Calculated Property
η 0.0012093 Pa×s 343.35 Calculated Property
η 0.0009712 Pa×s 366.54 Calculated Property
η 0.0008006 Pa×s 389.74 Calculated Property
η 0.0006745 Pa×s 412.94 Calculated Property
η 0.0005787 Pa×s 436.13 Calculated Property
η 0.0005042 Pa×s 459.33 Calculated Property
η 0.0004452 Pa×s 482.53 Calculated Property
η 0.0003976 Pa×s 505.72 Calculated Property
η 0.0003587 Pa×s 528.92 Calculated Property

Similar Compounds

Oxirane, (phenoxymethyl)-. p-Chlorophenyl 2,3-epoxypropyl ether. Oxirane, 2,2'-[1,3-phenylenebis(oxymethylene)]bis-. p-Cresyl glycidyl ether. Oxirane, [[4-(1,1-dimethylethyl)phenoxy]methyl]-. Oxirane, [(2-methylphenoxy)methyl]-. Bis[4-[(oxiran-2-yl)methoxy]phenyl]methane. 1,2-PROPANEDIOL, 3-(4-CHLOROPHENOXY)-. 1,2-Propanediol, 3-phenoxy-. 1-Phenoxypropan-2-ol. Oxirane, 2,2'-[(1-methylethylidene)bis(4,1-phenyleneoxymethylene)]bis-. 2,2-Bis(phenyl-4-glycidoxy)propane. 1,2-Propanediol, 3-(2-methoxyphenoxy)-. 1-Phenoxypropan-2-yl acetate. 2-BIPHENYLYL 2,3-EPOXYPROPYL ETHER.

Find more compounds similar to 2,3-Epoxypropyl-p-methoxyphenylether.

Sources

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