Chemical Properties of Cyclopropane, 1-methoxy-2,3-dimethyl- (CAS 116405-11-9)

Cyclopropane, 1-methoxy-2,3-dimethyl-

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InChI
InChI=1S/C6H12O/c1-4-5(2)6(4)7-3/h4-6H,1-3H3
InChI Key
SRXMDYKINVQGHW-UHFFFAOYSA-N
Formula
C6H12O
SMILES
COC1C(C)C1C
Molecular Weight1
100.16
CAS
116405-11-9
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Physical Properties

Property Value Unit Source
Δf -60.03 kJ/mol Joback Calculated Property
Δfgas -267.27 kJ/mol Joback Calculated Property
Δfus 12.76 kJ/mol Joback Calculated Property
Δvap 30.66 kJ/mol Joback Calculated Property
log10WS -0.94 Crippen Calculated Property
logPoct/wat 1.287 Crippen Calculated Property
McVol 90.410 ml/mol McGowan Calculated Property
Pc 3276.53 kPa Joback Calculated Property
Tboil 356.50 K Joback Calculated Property
Tc 534.33 K Joback Calculated Property
Tfus 189.07 K Joback Calculated Property
Vc 0.344 m3/kmol Joback Calculated Property

Temperature Dependent Properties

Property Value Unit Temperature (K) Source
Cp,gas [165.46; 231.17] J/mol×K [356.50; 534.33] Show Hide
Cp,gas 165.46 J/mol×K 356.50 Joback Calculated Property
Cp,gas 177.46 J/mol×K 386.14 Joback Calculated Property
Cp,gas 189.03 J/mol×K 415.78 Joback Calculated Property
Cp,gas 200.18 J/mol×K 445.41 Joback Calculated Property
Cp,gas 210.92 J/mol×K 475.05 Joback Calculated Property
Cp,gas 221.25 J/mol×K 504.69 Joback Calculated Property
Cp,gas 231.17 J/mol×K 534.33 Joback Calculated Property
η [0.0002122; 0.0002196] Pa×s [189.07; 356.50] Show Hide
η 0.0002122 Pa×s 189.07 Joback Calculated Property
η 0.0002142 Pa×s 216.97 Joback Calculated Property
η 0.0002158 Pa×s 244.88 Joback Calculated Property
η 0.0002170 Pa×s 272.78 Joback Calculated Property
η 0.0002180 Pa×s 300.69 Joback Calculated Property
η 0.0002189 Pa×s 328.60 Joback Calculated Property
η 0.0002196 Pa×s 356.50 Joback Calculated Property

Similar Compounds

7-Methoxynorcarane. 3-Methoxy-4-methylheptane. Butane, 2-methoxy-3-methyl-. 2,4-Dimethyltetrahydrofuran. Furan, tetrahydro-2,4-dimethyl-, cis-. Furan, tetrahydro-2,4-dimethyl-, trans-. Tricyclo[3.3.1.1(3,7)]decane, 2-methoxy-. Tricyclo[4.3.1.1(2,5)]undecane, 10-methoxy-, stereoisomer. Formic acid, 2-methylhex-3-yl ester. Formic acid, 2,4-dimethylpent-3-yl ester. Exo-2-methyl-7-oxabi-cyclo[2.2.1]heptane. Endo-2-methyl-7-oxabi-cyclo[2.2.1]heptane. 4-Methyl-2-pentanol, methyl ether. Furan, tetrahydro-2,2-dimethyl-5-(1-methylpropyl)-. Nortricyclyl formate.

Find more compounds similar to Cyclopropane, 1-methoxy-2,3-dimethyl-.

Sources

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