Chemical Properties of 1-(4-methylthiophenyl)-2-propanone

1-(4-methylthiophenyl)-2-propanone

InChI
InChI=1S/C10H12OS/c1-8(11)7-9-3-5-10(12-2)6-4-9/h3-6H,7H2,1-2H3
InChI Key
RYFZDEIJXAESAA-UHFFFAOYSA-N
Formula
C10H12OS
SMILES
CSc1ccc(CC(C)=O)cc1
Molecular Weight1
180.27
Other Names
  • 4-Methylthioamphetamine -M (deamino oxo-)
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Physical Properties

Property Value Unit Source
ω 0.4515 Relay (1.0) Calculated Property
Δf 40.30 kJ/mol Joback Calculated Property
Δfgas -107.79 kJ/mol Relay (1.0) Calculated Property
Δfus 21.04 kJ/mol Joback Calculated Property
Δvap 67.00 kJ/mol Relay (1.0) Calculated Property
IE 7.94 eV Relay (1.0) Calculated Property
log10WS -2.40 Relay (1.0) Calculated Property
logPoct/wat 2.540 Crippen Calculated Property
McVol 145.920 ml/mol McGowan Calculated Property
Pc 3149.09 kPa Joback Calculated Property
Tboil 562.35 K Relay (1.0) Calculated Property
Tc 759.35 K Relay (1.0) Calculated Property
Tfus 319.65 K Relay (1.0) Calculated Property
Vc 0.504 m3/kmol Relay (1.0) Calculated Property

Temperature Dependent Properties

Property Value Unit Temperature (K) Source
Cp,gas [326.39; 395.37] J/mol×K [582.51; 818.40] Show Hide
Cp,gas 326.39 J/mol×K 582.51 Joback Calculated Property
Cp,gas 340.06 J/mol×K 621.83 Joback Calculated Property
Cp,gas 352.82 J/mol×K 661.14 Joback Calculated Property
Cp,gas 364.70 J/mol×K 700.46 Joback Calculated Property
Cp,gas 375.74 J/mol×K 739.77 Joback Calculated Property
Cp,gas 385.95 J/mol×K 779.09 Joback Calculated Property
Cp,gas 395.37 J/mol×K 818.40 Joback Calculated Property

Similar Compounds

Benzyl methyl ketone. 4-Methylphenyl acetone. p-(Chlorophenyl)acetone. 2-Propanone, 1,3-diphenyl-. (4-Fluorophenyl)acetone. 1-Phenyl-2-butanone. 4-Nitrophenylacetone. 2-Propanone, 1-(4-methoxyphenyl)-. 1-hydroxy-3-phenyl-2-propanone. Sulfide, phenyl 3-phenylpropyl. 2-Propanone, 1-[3-(trifluoromethyl)phenyl]-. 2-Pentanone, 1-phenyl-. 1-(4-Methylthiophenyl)-2-propanol, acetate. 3-Methoxyphenyl acetone. 1-Phenyl-2-hexanone.

Find more compounds similar to 1-(4-methylthiophenyl)-2-propanone.

Sources

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