Chemical Properties of 5,5-Dibromobarbituric acid

5,5-Dibromobarbituric acid

InChI
InChI=1S/C4H2Br2N2O3/c5-4(6)1(9)7-3(11)8-2(4)10/h(H2,7,8,9,10,11)
InChI Key
AMATXUCYHHHHHB-UHFFFAOYSA-N
Formula
C4H2Br2N2O3
SMILES
O=C1NC(=O)C(Br)(Br)C(=O)N1
Molecular Weight1
285.88
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Physical Properties

Property Value Unit Source
Δfus 19.93 kJ/mol Joback Calculated Property
IE 10.24 eV Relay (1.0) Calculated Property
log10WS -2.31 Relay (1.0) Calculated Property
logPoct/wat -0.162 Crippen Calculated Property
McVol 116.030 ml/mol McGowan Calculated Property
Tfus 524.10 K Relay (1.0) Calculated Property

Cheméo can also estimate Normal Boiling Point Temperature, Critical Temperature, Critical Pressure, Critical Volume, Enthalpy of formation at standard conditions, Enthalpy of vaporization at standard conditions, Standard Gibbs free energy of formation, Acentric Factor for this compound, but they fall outside the models' validated range, so they are not shown here. Open the prediction tool to compute them on demand.

Temperature Dependent Properties

Property Value Unit Temperature (K) Source
Cp,gas [247.30; 306.25] J/mol×K [743.79; 1061.24] Show Hide
Cp,gas 247.30 J/mol×K 743.79 Joback Calculated Property
Cp,gas 258.21 J/mol×K 796.70 Joback Calculated Property
Cp,gas 268.68 J/mol×K 849.61 Joback Calculated Property
Cp,gas 278.71 J/mol×K 902.52 Joback Calculated Property
Cp,gas 288.31 J/mol×K 955.43 Joback Calculated Property
Cp,gas 297.49 J/mol×K 1008.34 Joback Calculated Property
Cp,gas 306.25 J/mol×K 1061.24 Joback Calculated Property

Similar Compounds

2,4,5,6(1H,3H)-PYRIMIDINETETRONE. Barbituric acid. Violuric acid. 5,5-dimethylbarbituric acid. 5-Methylbarbituric acid. 5,5-DIHYDROXY-2,4,6(1H,3H,5H)-PYRIMIDINETRIONE. 2,4,6(1H,3H,5H)-Pyrimidinetrione, 5-hydroxy-. Uramil. Acetylcarbromal. 5-ethyl-1,3-diazinane-2,4,6-trione. Isopropylbarbituric acid. 2,4(1H,3H)-Pyrimidinedione, dihydro-. 5-ethyl-5-methyl-1,3-diazinane-2,4,6-trione. 5,7-Diazaspiro[2.5]octane-4,6,8-trione. Barbital.

Find more compounds similar to 5,5-Dibromobarbituric acid.

Sources

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