Chemical Properties of Propanoic acid, 3-hydroxy-2[3-(2-chloroethyl)ureido]-

Propanoic acid, 3-hydroxy-2[3-(2-chloroethyl)ureido]-

InChI
InChI=1S/C6H11ClN2O4/c7-1-2-8-6(13)9-4(3-10)5(11)12/h4,10H,1-3H2,(H,11,12)(H2,8,9,13)
InChI Key
SSAHXIIXIQFLMV-UHFFFAOYSA-N
Formula
C6H11ClN2O4
SMILES
O=C(NCCCl)NC(CO)C(=O)O
Molecular Weight1
210.62
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Physical Properties

Property Value Unit Source
Δfus 38.00 kJ/mol Joback Calculated Property
logPoct/wat -1.030 Crippen Calculated Property
McVol 142.480 ml/mol McGowan Calculated Property

Cheméo can also estimate Normal Boiling Point Temperature, Normal melting (fusion) point, 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, Ionization energy, Log10 of Water solubility in mol/l 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 [388.27; 424.79] J/mol×K [765.77; 963.60] Show Hide
Cp,gas 388.27 J/mol×K 765.77 Joback Calculated Property
Cp,gas 395.49 J/mol×K 798.74 Joback Calculated Property
Cp,gas 402.22 J/mol×K 831.71 Joback Calculated Property
Cp,gas 408.49 J/mol×K 864.69 Joback Calculated Property
Cp,gas 414.32 J/mol×K 897.66 Joback Calculated Property
Cp,gas 419.75 J/mol×K 930.63 Joback Calculated Property
Cp,gas 424.79 J/mol×K 963.60 Joback Calculated Property

Similar Compounds

Serine, n-(2-imidazolin-2-yl)-. Glutaramic acid, 2-[3-(2-chloroethyl)ureido]-, l(-). Glutamic acid, n-[(2-chloroethyl)carbamoyl]-, dimethyl ester. Emetine. Adenosine, 5'-S-methyl-5'-thio-. Uridine, 5,6-dihydro-. Levallorphan. 5-Methyluridine. Norlevorphanol. (+)-Roemerine. Spiro[2,5-cyclohexadiene-1,7'(1'H)-cyclopent[ij]isoquinolin]-4-one, 2',3',8',8'a-tetrahydro-5',6'-dimethoxy-1'-methyl-, (R)-. 5-Methyluridine, tris(trimethylsilyl) deriv.. (-)-2-Aminobutan-1-ol, ferroceneboronate derivative. Metopon. N-Acetylnornarcotine.

Find more compounds similar to Propanoic acid, 3-hydroxy-2[3-(2-chloroethyl)ureido]-.

Sources

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