Chemical Properties of 9-Fluorenone-2-carboxylic acid (CAS 784-50-9)

9-Fluorenone-2-carboxylic acid

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InChI
InChI=1S/C14H8O3/c15-13-11-4-2-1-3-9(11)10-6-5-8(14(16)17)7-12(10)13/h1-7H,(H,16,17)
InChI Key
BJCTXUUKONLPPK-UHFFFAOYSA-N
Formula
C14H8O3
SMILES
O=C(O)c1ccc2c(c1)C(=O)c1ccccc1-2
Molecular Weight1
224.21
CAS
784-50-9
Other Names
  • Fluorenone-2-carboxylic acid
  • 9H-Fluorene-2-carboxylic acid, 9-oxo-
  • 9-Oxo-2-fluorenecarboxylic acid
  • 9-oxofluoren-2-carboxylic acid
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Physical Properties

Property Value Unit Source
Δf -32.74 kJ/mol Joback Calculated Property
Δfgas -190.69 kJ/mol Joback Calculated Property
Δfus 25.39 kJ/mol Joback Calculated Property
Δvap 80.85 kJ/mol Joback Calculated Property
log10WS -4.34 Crippen Calculated Property
logPoct/wat 2.596 Crippen Calculated Property
McVol 158.750 ml/mol McGowan Calculated Property
Pc 3708.97 kPa Joback Calculated Property
Tboil 804.76 K Joback Calculated Property
Tc 1043.25 K Joback Calculated Property
Tfus 546.13 K Joback Calculated Property
Vc 0.610 m3/kmol Joback Calculated Property

Temperature Dependent Properties

Property Value Unit Temperature (K) Source
Cp,gas [430.37; 479.43] J/mol×K [804.76; 1043.25] Show Hide
Cp,gas 430.37 J/mol×K 804.76 Joback Calculated Property
Cp,gas 439.96 J/mol×K 844.51 Joback Calculated Property
Cp,gas 448.88 J/mol×K 884.26 Joback Calculated Property
Cp,gas 457.21 J/mol×K 924.01 Joback Calculated Property
Cp,gas 465.02 J/mol×K 963.76 Joback Calculated Property
Cp,gas 472.41 J/mol×K 1003.50 Joback Calculated Property
Cp,gas 479.43 J/mol×K 1043.25 Joback Calculated Property

Similar Compounds

9-Fluorenone-4-carboxylic acid. 2,7-Diacetyl-9-fluorenone. 3-Methyl-9-fluorenone. 9H-Fluoren-9-one. Fluorene-4-carboxylic acid. 11H-benzo[b]fluorene-11-one. 2-Nitro-9-fluorenone. 7-methyl-4-azafluorenone. 7H-Benzo[c]fluoren-7-one. 11H-Benzo[a]fluoren-11-one. 4-Hydroxy-9-fluorenone. 9H-Fluoren-9-one, 3-nitro-. 9H-Fluoren-9-one, 2,7-dinitro-. Fluoren-9-one, 3-bromo-. Fluoren-9-one, 2-ethylamino-.

Find more compounds similar to 9-Fluorenone-2-carboxylic acid.

Sources

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