Chemical Properties of Oxirane, [(2-methylphenoxy)methyl]- (CAS 2210-79-9)

InChI

InChI=1S/C10H12O2/c1-8-4-2-3-5-10(8)12-7-9-6-11-9/h2-5,9H,6-7H2,1H3

InChI Key

KFUSXMDYOPXKKT-UHFFFAOYSA-N

Formula

C10H12O2

SMILES

Cc1ccccc1OCC1CO1

Molecular Weight¹

164.20

CAS

2210-79-9

Other Names

• o-Cresol glycidyl ether
• 3-(2-Methylphenoxy)-1,2-epoxypropane
• o-Cresyl glycidyl ether
• o-Kresol-glycidaether
• Glycidyl o-tolyl ether
• Glycidyl 2-methylphenyl ether
• Propane, 1,2-epoxy-3-(o-tolyloxy)-
• Propane, 1,2-epoxy-3-(o-tolyoxy)-
• 1-(o-Methylphenoxy)-2,3-epoxypropane
• 1-(2-Methylphenoxy)-2,3-epoxypropane
• 1,2-Epoxy-3-(o-tolyoxy)propane
• 1,2-Epoxy-3-(2-methylphenoxy)propane
• 2-((2-Methylphenoxy)methyl)oxirane
• 1,2-Epoxy-3-(o-tolyloxy)propane
• Glycidyl o-methylphenyl ether
• 2-Methylphenyl glycidyl ether
• 1-(2,3-Epoxypropoxy)-2-methylbenzene
• ((2-Methylphenoxy)methyl)oxirane
• Cresol, o-epoxypropyl ether
• Heloxy 62
• o-Tolyl epoxypropyl ether
• o-Tolyl glycidyl ether
• Araldite DY 023
• NSC 11571
• NSC 20291
• Oxirane, 2-[(2-methylphenoxy)methyl]-
• 2,3-epoxypropyl o-tolyl ether

• ω : Acentric Factor.
• C_p,gas : Ideal gas heat capacity (J/mol×K).
• η : Dynamic viscosity (Pa×s).
• Δ_fG° : Standard Gibbs free energy of formation (kJ/mol).
• Δ_fH°_gas : Enthalpy of formation at standard conditions (kJ/mol).
• Δ_fusH° : Enthalpy of fusion at standard conditions (kJ/mol).
• Δ_vapH° : Enthalpy of vaporization at standard conditions (kJ/mol).
• IE : Ionization energy (eV).
• log₁₀WS : Log10 of Water solubility in mol/l.
• logP_oct/wat : Octanol/Water partition coefficient.
• McVol : McGowan's characteristic volume (ml/mol).
• P_c : Critical Pressure (kPa).
• T_boil : Normal Boiling Point Temperature (K).
• T_boilr : Boiling point at reduced pressure (K).
• T_c : Critical Temperature (K).
• T_fus : Normal melting (fusion) point (K).
• V_c : Critical Volume (m³/kmol).
• ¹: Molecular weight from the IUPAC atomic weights tables.

Physical Properties

Temperature Dependent Properties

Property	Value	Unit	Temperature (K)	Source
Cp,gas	[296.69; 372.56]	J/mol×K	[515.97; 735.33]
Cp,gas	296.69	J/mol×K	515.97	Joback Calculated Property
Cp,gas	311.47	J/mol×K	552.53	Joback Calculated Property
Cp,gas	325.34	J/mol×K	589.09	Joback Calculated Property
Cp,gas	338.35	J/mol×K	625.65	Joback Calculated Property
Cp,gas	350.52	J/mol×K	662.21	Joback Calculated Property
Cp,gas	361.91	J/mol×K	698.77	Joback Calculated Property
Cp,gas	372.56	J/mol×K	735.33	Joback Calculated Property
η	[0.0004015; 0.0016203]	Pa×s	[308.14; 515.97]
η	0.0016203	Pa×s	308.14	Joback Calculated Property
η	0.0011418	Pa×s	342.78	Joback Calculated Property
η	0.0008580	Pa×s	377.42	Joback Calculated Property
η	0.0006764	Pa×s	412.06	Joback Calculated Property
η	0.0005534	Pa×s	446.69	Joback Calculated Property
η	0.0004659	Pa×s	481.33	Joback Calculated Property
η	0.0004015	Pa×s	515.97	Joback Calculated Property

Pressure Dependent Properties

Similar Compounds

Find more compounds similar to Oxirane, [(2-methylphenoxy)methyl]-.

Sources

• Cheméo Relay (1.0)
• Crippen Method
• Crippen Method
• Joback Method
• McGowan Method
• NIST Webbook

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