Chemical Properties of Anthranilic acid, n-glycoloyl-n-methyl- (CAS 116295-99-9)

Anthranilic acid, n-glycoloyl-n-methyl-

InChI
InChI=1S/C10H11NO4/c1-11(9(13)6-12)8-5-3-2-4-7(8)10(14)15/h2-5,12H,6H2,1H3,(H,14,15)
InChI Key
SPDMHQSMCGQLDG-UHFFFAOYSA-N
Formula
C10H11NO4
SMILES
CN(C(=O)CO)c1ccccc1C(=O)O
Molecular Weight1
209.20
CAS
116295-99-9
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Physical Properties

Property Value Unit Source
ΔfH°gas -618.94 kJ/mol Relay (1.0) Calculated Property
ΔfusH° 34.16 kJ/mol Joback Calculated Property
ΔvapH° 109.72 kJ/mol Relay (1.0) Calculated Property
IE 8.84 eV Relay (1.0) Calculated Property
log10WS -0.73 Relay (1.0) Calculated Property
logPoct/wat 0.340 Crippen Calculated Property
McVol 152.860 ml/mol McGowan Calculated Property
Tboil 596.62 K Relay (1.0) Calculated Property
Tc 915.35 K Relay (1.0) Calculated Property
Tfus 423.70 K Relay (1.0) Calculated Property

Cheméo can also estimate Critical Pressure, Critical Volume, 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.

Correlations

Property Value Unit Temperature (K) Source
Cp,gas [205.47; 470.17] J/mol×K [273.00; 1000.00] Joback Predicted correlation Show Hide
EquationY = A + B·T + C·T² + D·T³ + E·T⁴
Y is Cp,gas in J/mol×K, T in K
Coefficient A-1.92490e+01
Coefficient B9.96120e-01
Coefficient C-6.81260e-04
Coefficient D1.74560e-07
Coefficient E0.00000e+00
Temperature range, min.273.00
Temperature range, max.1000.00
Cp,gas 205.47 J/mol×K 273.00 Calculated Property
Cp,gas 255.62 J/mol×K 353.78 Calculated Property
Cp,gas 299.30 J/mol×K 434.56 Calculated Property
Cp,gas 337.05 J/mol×K 515.33 Calculated Property
Cp,gas 369.44 J/mol×K 596.11 Calculated Property
Cp,gas 397.01 J/mol×K 676.89 Calculated Property
Cp,gas 420.32 J/mol×K 757.67 Calculated Property
Cp,gas 439.91 J/mol×K 838.44 Calculated Property
Cp,gas 456.35 J/mol×K 919.22 Calculated Property
Cp,gas 470.17 J/mol×K 1000.00 Calculated Property

Similar Compounds

5H-4,1-benzoxazepine-2,5-dione,1,2-dihydro-1-methyl-,. 3H-1,4-benzodiazepine-2,5-dione, 1,2,4,5-tetrahydro-1-methyl-4-phenyl-. Diazepam, M(HO-), acid hydrolyzed, acetylated. 3H-1,4-benzodiazepine-2,5-dione,4-(p-chlorophenyl)-1,2,4,5-tetrahydro-1-methyl-. 3H-1,4-benzodiazepine-2,5-dione, 8-chloro-1,2,4,5-tetrahydro-1,4-dimethyl-. Benzoic acid, 2-di(3-methylbutyl)amino-, methyl ester. Benzanilide, 2-(n-methyl-chloroacetamido)-. 3H-1,4-benzodiazepine-2,5-dione, 7-chloro-1,2,4,5-tetrahydro-1,4-dimethyl-. Flurazepam M (hydroxyethyl-), hydrolysis, acetylated. Halazepam M (hydroxy-), isomer 2, hydrolysis, acetylated. 2H-1,4-Benzodiazepin-2-one, 1,3-dihydro-7-chloro-5-(2-fluorophenyl)-1-(2-hydroxyethyl)-. HYDROXYETHYLFLURAZEPAM. vasicinone. 2-Naphthanilide, 4-[4-diethylamino-o-tolylimino]-1,4-dihydro-n-methyl-1-oxo-. Tetrazepam M (hydroxy-), isomer 2, hydrolysis, acetylated.

Find more compounds similar to Anthranilic acid, n-glycoloyl-n-methyl-.

Sources

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