Chemical Properties of Naphthalene, 1,2-dihydro-1,4,6-trimethyl- (CAS 55682-80-9)

Naphthalene, 1,2-dihydro-1,4,6-trimethyl-

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InChI
InChI=1S/C13H16/c1-9-4-7-12-10(2)5-6-11(3)13(12)8-9/h4,6-8,10H,5H2,1-3H3
InChI Key
HQBMLUDYOSJUOR-UHFFFAOYSA-N
Formula
C13H16
SMILES
CC1=CCC(C)c2ccc(C)cc21
Molecular Weight1
172.27
CAS
55682-80-9
Other Names
  • 1,2-Dihydro-1,4,6-trimethylnaphthalene
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Physical Properties

Property Value Unit Source
Δf 220.71 kJ/mol Joback Calculated Property
Δfgas 14.89 kJ/mol Joback Calculated Property
Δfus 19.56 kJ/mol Joback Calculated Property
Δvap 49.17 kJ/mol Joback Calculated Property
log10WS -4.27 Crippen Calculated Property
logPoct/wat 3.906 Crippen Calculated Property
McVol 155.110 ml/mol McGowan Calculated Property
Pc 2527.73 kPa Joback Calculated Property
Inp 1373.40 NIST
Tboil 548.63 K Joback Calculated Property
Tc 773.57 K Joback Calculated Property
Tfus 315.43 K Joback Calculated Property
Vc 0.591 m3/kmol Joback Calculated Property

Temperature Dependent Properties

Property Value Unit Temperature (K) Source
Cp,gas [362.42; 451.75] J/mol×K [548.63; 773.57] Show Hide
Cp,gas 362.42 J/mol×K 548.63 Joback Calculated Property
Cp,gas 379.80 J/mol×K 586.12 Joback Calculated Property
Cp,gas 396.11 J/mol×K 623.61 Joback Calculated Property
Cp,gas 411.41 J/mol×K 661.10 Joback Calculated Property
Cp,gas 425.75 J/mol×K 698.59 Joback Calculated Property
Cp,gas 439.18 J/mol×K 736.08 Joback Calculated Property
Cp,gas 451.75 J/mol×K 773.57 Joback Calculated Property
η [0.0003143; 0.0012357] Pa×s [315.43; 548.63] Show Hide
η 0.0012357 Pa×s 315.43 Joback Calculated Property
η 0.0008679 Pa×s 354.30 Joback Calculated Property
η 0.0006536 Pa×s 393.16 Joback Calculated Property
η 0.0005181 Pa×s 432.03 Joback Calculated Property
η 0.0004267 Pa×s 470.90 Joback Calculated Property
η 0.0003620 Pa×s 509.76 Joback Calculated Property
η 0.0003143 Pa×s 548.63 Joback Calculated Property

Similar Compounds

Calacorene. «alpha»-Calacorene. «gamma»-Calacorene. 18-Hydroxyoestrone (enol), TMS. 16-Ketoestradiol (enol), TMS. 17«beta»-16-oxo-Oestradiol, TMS. Cinchonidine. Cinchonine. Tetrahydrocannabinol. 11B-Hydroxyoestrone (enol), TMS. 3-Ethoxycarbonyl-17-oxaestra-1,3,5(10)-trien-16-one. Dimetindene M (nor, OH), acetylated. 11B-Hydroxyoestradiol, TMS. 6-Dehydroestradiol, TMS. Estra-1,3,5(10),6-tetraene-3,17-diol, (17«beta»)-.

Find more compounds similar to Naphthalene, 1,2-dihydro-1,4,6-trimethyl-.

Sources

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