Chemical Properties of 1,3-Dioxane, 2-ethyl-4-pentyl, 2R,4R

1,3-Dioxane, 2-ethyl-4-pentyl, 2R,4R

Download as PDF file Download as Excel file Download as 2D mole file Predict properties

InChI
InChI=1S/C11H22O2/c1-3-5-6-7-10-8-9-12-11(4-2)13-10/h10-11H,3-9H2,1-2H3/t10-,11-/m0/s1
InChI Key
UCGYQTHBPZXKHC-QWRGUYRKSA-N
Formula
C11H22O2
SMILES
CCCCCC1CCOC(CC)O1
Molecular Weight1
186.29

Physical Properties

Property Value Unit Source
Δf -113.76 kJ/mol Joback Calculated Property
Δfgas -500.39 kJ/mol Joback Calculated Property
Δfus 33.11 kJ/mol Joback Calculated Property
Δvap 49.22 kJ/mol Joback Calculated Property
log10WS -3.22 Crippen Calculated Property
logPoct/wat 3.108 Crippen Calculated Property
McVol 166.730 ml/mol McGowan Calculated Property
Pc 2224.99 kPa Joback Calculated Property
I [1560.00; 1560.00]   Show Hide
I 1560.00 NIST
I 1560.00 NIST
Tboil 519.86 K Joback Calculated Property
Tc 712.81 K Joback Calculated Property
Tfus 270.01 K Joback Calculated Property
Vc 0.625 m3/kmol Joback Calculated Property

Temperature Dependent Properties

Property Value Unit Temperature (K) Source
Cp,gas [416.76; 518.84] J/mol×K [519.86; 712.81] Show Hide
Cp,gas 416.76 J/mol×K 519.86 Joback Calculated Property
Cp,gas 435.96 J/mol×K 552.02 Joback Calculated Property
Cp,gas 454.26 J/mol×K 584.18 Joback Calculated Property
Cp,gas 471.69 J/mol×K 616.34 Joback Calculated Property
Cp,gas 488.24 J/mol×K 648.49 Joback Calculated Property
Cp,gas 503.96 J/mol×K 680.65 Joback Calculated Property
Cp,gas 518.84 J/mol×K 712.81 Joback Calculated Property
η [0.0002794; 0.0055245] Pa×s [270.01; 519.86] Show Hide
η 0.0055245 Pa×s 270.01 Joback Calculated Property
η 0.0024098 Pa×s 311.65 Joback Calculated Property
η 0.0012782 Pa×s 353.29 Joback Calculated Property
η 0.0007750 Pa×s 394.94 Joback Calculated Property
η 0.0005170 Pa×s 436.58 Joback Calculated Property
η 0.0003700 Pa×s 478.22 Joback Calculated Property
η 0.0002794 Pa×s 519.86 Joback Calculated Property

Similar Compounds

1,3-Dioxane, 2-ethyl-4-pentyl, 2S,4R. 1,3-Dioxane, 2-propyl-4-pentyl, 2S,4R. 1,3-Dioxane, 2-propyl-4-pentyl, 2R,4R. 1,3-Dioxane, 2,4-dipentyl, 2S,4R. 1,3-Dioxane, 2,4-pentyl, 2R,4R. 1,3-Dioxane, 2-isopropyl-4-pentyl, 2R,4R. 1,3-Dioxane, 2-isopropyl-4-pentyl, 2S,4R. 1,3-Dioxane, 2-isopentyl-4-pentyl, 2R,4R. 1,3-Dioxane, 2-isopentyl-4-pentyl, 2S,4R. 1,3-Dioxane, 2-ethyl-2-methyl-4-pentyl, 2S,4R. 1,3-Dioxane, 2-ethyl-2methyl-4-pentyl, 2R,4R. 1,3-Dioxane, 2-(1-methylbutyl)-4-pentyl, 2S,4R. 1,3-Dioxane, 2-(1-methylbutyl)-4-pentyl, 2R,4R. 1,3-Dioxane, 2,2-dimethyl-4-pentyl, 4R. 1,3-Dioxane, 2-methyl-4-(4-hydroxypentyl), 2S,4R.

Find more compounds similar to 1,3-Dioxane, 2-ethyl-4-pentyl, 2R,4R.

Sources

Note: Cheméo is only indexing the data, follow the source links to retrieve the latest data. The source is also providing more information like the publication year, authors and more. Take the time to validate and double check the source of the data.

Login Register