Chemical Properties of 2,4,6(1H,3H,5H)-Pyrimidinetrione, 5-hydroxy- (CAS 444-15-5)

2,4,6(1H,3H,5H)-Pyrimidinetrione, 5-hydroxy-

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InChI
InChI=1S/C4H4N2O4/c7-1-2(8)5-4(10)6-3(1)9/h1,7H,(H2,5,6,8,9,10)
InChI Key
BVEWMNTVZPFPQI-UHFFFAOYSA-N
Formula
C4H4N2O4
SMILES
O=C1NC(=O)C(O)C(=O)N1
Molecular Weight1
144.09
CAS
444-15-5
Other Names
  • 5-Hydroxy-2,4,6(1h,3h,5h)-pyrimidinetrione
  • 5-hydroxybarbituric acid
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Physical Properties

Property Value Unit Source
Δf -321.92 kJ/mol Joback Calculated Property
Δfgas -561.28 kJ/mol Joback Calculated Property
Δfus 19.75 kJ/mol Joback Calculated Property
Δvap 67.86 kJ/mol Joback Calculated Property
log10WS 0.55 Crippen Calculated Property
logPoct/wat -2.287 Crippen Calculated Property
McVol 86.900 ml/mol McGowan Calculated Property
Pc 7561.44 kPa Joback Calculated Property
Tboil 703.21 K Joback Calculated Property
Tc 955.99 K Joback Calculated Property
Tfus 617.76 K Joback Calculated Property
Vc 0.306 m3/kmol Joback Calculated Property

Temperature Dependent Properties

Property Value Unit Temperature (K) Source
Cp,gas [237.46; 285.82] J/mol×K [703.21; 955.99] Show Hide
Cp,gas 237.46 J/mol×K 703.21 Joback Calculated Property
Cp,gas 248.11 J/mol×K 745.34 Joback Calculated Property
Cp,gas 257.92 J/mol×K 787.47 Joback Calculated Property
Cp,gas 266.76 J/mol×K 829.60 Joback Calculated Property
Cp,gas 274.46 J/mol×K 871.73 Joback Calculated Property
Cp,gas 280.86 J/mol×K 913.86 Joback Calculated Property
Cp,gas 285.82 J/mol×K 955.99 Joback Calculated Property

Similar Compounds

2,4,6(1H,3H,5H)-Pyrimidinetrione, 5,5-dihydroxy-. Barbituric acid. Uroxine. Barbituric acid, 5-hydroxy-5-thiosemicarbazido-. 5-Methylbarbituric acid. Isopropylbarbituric acid. Uramil. 2,4(1H,3H)-Pyrimidinedione, dihydro-. Barbituric acid, 5-nitro-. 5-ethyl-1,3-diazinane-2,4,6-trione. 1,5-Dimethylbarbituric acid. 5,6-Dihydro-5-methyluracil. 5,6-Dihydro-6-methyluracil. Barbituric acid, 5-allyl-. 2,4,6(1H,3H,5H)-Pyrimidinetrione, 5-phenyl-1-(phenylmethyl)-.

Find more compounds similar to 2,4,6(1H,3H,5H)-Pyrimidinetrione, 5-hydroxy-.

Sources

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