Chemical Properties of 1-Methylthymine (CAS 4160-72-9)

1-Methylthymine

InChI
InChI=1S/C6H8N2O2/c1-4-3-8(2)6(10)7-5(4)9/h3H,1-2H3,(H,7,9,10)
InChI Key
GKMIDMKPBOUSBQ-UHFFFAOYSA-N
Formula
C6H8N2O2
SMILES
Cc1cn(C)c(=O)[nH]c1=O
Molecular Weight1
140.14
CAS
4160-72-9
Other Names
  • 1,5-dimethyluracil
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Physical Properties

Property Value Unit Source
ω 0.5370 Relay (1.0) Calculated Property
EA 0.04 ± 0.01 eV NIST
Δf -38.55 kJ/mol Relay (1.0-beta) Calculated Property
Δfgas -320.77 kJ/mol Relay (1.0) Calculated Property
Δvap 89.99 kJ/mol Relay (1.0) Calculated Property
IE 8.61 eV Relay (1.0) Calculated Property
log10WS 0.31 Relay (1.0) Calculated Property
logPoct/wat -1.100 Crippen Calculated Property
McVol 103.340 ml/mol McGowan Calculated Property
Pc 5066.46 kPa Relay (1.0-beta) Calculated Property
Tboil 565.98 K Relay (1.0) Calculated Property
Tc 764.06 K Relay (1.0) Calculated Property
Tfus 484.26 K Relay (1.0) Calculated Property
Vc 0.387 m3/kmol Relay (1.0) Calculated Property

Temperature Dependent Properties

Property Value Unit Temperature (K) Source
Cp,solid [187.60; 205.20] J/mol×K [298.15; 343.15] Show Hide
Cp,solid 187.60 J/mol×K 298.15 Heat Capacities of Uracil, Thymine, and Its Alkylated, Cyclooligomethylenated, and Halogenated Derivatives by Differential Calorimetry
Cp,solid 190.00 J/mol×K 303.15 Heat Capacities of Uracil, Thymine, and Its Alkylated, Cyclooligomethylenated, and Halogenated Derivatives by Differential Calorimetry
Cp,solid 190.30 J/mol×K 308.15 Heat Capacities of Uracil, Thymine, and Its Alkylated, Cyclooligomethylenated, and Halogenated Derivatives by Differential Calorimetry
Cp,solid 194.10 J/mol×K 313.15 Heat Capacities of Uracil, Thymine, and Its Alkylated, Cyclooligomethylenated, and Halogenated Derivatives by Differential Calorimetry
Cp,solid 194.80 J/mol×K 318.15 Heat Capacities of Uracil, Thymine, and Its Alkylated, Cyclooligomethylenated, and Halogenated Derivatives by Differential Calorimetry
Cp,solid 198.50 J/mol×K 323.15 Heat Capacities of Uracil, Thymine, and Its Alkylated, Cyclooligomethylenated, and Halogenated Derivatives by Differential Calorimetry
Cp,solid 199.20 J/mol×K 328.15 Heat Capacities of Uracil, Thymine, and Its Alkylated, Cyclooligomethylenated, and Halogenated Derivatives by Differential Calorimetry
Cp,solid 202.00 J/mol×K 333.15 Heat Capacities of Uracil, Thymine, and Its Alkylated, Cyclooligomethylenated, and Halogenated Derivatives by Differential Calorimetry
Cp,solid 203.00 J/mol×K 338.15 Heat Capacities of Uracil, Thymine, and Its Alkylated, Cyclooligomethylenated, and Halogenated Derivatives by Differential Calorimetry
Cp,solid 205.20 J/mol×K 343.15 Heat Capacities of Uracil, Thymine, and Its Alkylated, Cyclooligomethylenated, and Halogenated Derivatives by Differential Calorimetry
ΔsubH 124.40 ± 1.30 kJ/mol 403.00 NIST

Similar Compounds

2,4(1H,3H)-Pyrimidinedione, 1,3,5-trimethyl-. Uracil, 5-(methoxymethyl)-1,3-dimethyl-. 1,3-Dimethyl-5-ethyluracil. Uracil, 1-methyl-. 5-fluoro-1-(phenylmethyl)pyrimidine-2,4-dione. 5-fluoro-1-[(4-methoxyphenyl)methyl]pyrimidine-2,4-dione. 1-Methyl-5-fluorouracil. 5-fluoro-1-[(4-methylphenyl)methyl]pyrimidine-2,4-dione. 1-[(4-chlorophenyl)methyl]-5-fluoropyrimidine-2,4-dione. Uracil, 1-{p-[3-(2-chloroethyl)ureido]benzyl}-. Thymidine. cis-Phenanthrene, 9,10-dihydro-9-methyl-9,10-diol, 3,4-dimethoxy, diacetate. Thymidine, bis(trimethylsilyl) deriv.. Thymidine, 3',5'-bis-O-TMS. Uridine, 5-methyl-.

Find more compounds similar to 1-Methylthymine.

Sources

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