Chemical Properties of Acetamide, n-(2,2,2-trifluoro-1,1-bis(p-fluorophenyl)ethyl)- (CAS 2247-78-1)

Acetamide, n-(2,2,2-trifluoro-1,1-bis(p-fluorophenyl)ethyl)-

InChI
InChI=1S/C16H12F5NO/c1-10(23)22-15(16(19,20)21,11-2-6-13(17)7-3-11)12-4-8-14(18)9-5-12/h2-9H,1H3,(H,22,23)
InChI Key
LOOCAEGGZALYLF-UHFFFAOYSA-N
Formula
C16H12F5NO
SMILES
CC(=O)NC(c1ccc(F)cc1)(c1ccc(F)cc1)C(F)(F)F
Molecular Weight1
329.26
CAS
2247-78-1
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Physical Properties

Property Value Unit Source
ω 0.5728 Relay (1.0) Calculated Property
Δf -718.50 kJ/mol Joback Calculated Property
Δfgas -1010.41 kJ/mol Relay (1.0) Calculated Property
Δfus 31.77 kJ/mol Joback Calculated Property
Δvap 90.31 kJ/mol Relay (1.0) Calculated Property
IE 8.61 eV Relay (1.0) Calculated Property
log10WS -5.02 Relay (1.0) Calculated Property
logPoct/wat 3.907 Crippen Calculated Property
McVol 209.180 ml/mol McGowan Calculated Property
Pc 2005.50 kPa Joback Calculated Property
Tboil 592.54 K Relay (1.0) Calculated Property
Tc 833.94 K Relay (1.0) Calculated Property
Tfus 362.30 K Relay (1.0) Calculated Property
Vc 0.728 m3/kmol Relay (1.0) Calculated Property

Temperature Dependent Properties

Property Value Unit Temperature (K) Source
Cp,gas [588.18; 651.63] J/mol×K [722.73; 934.92] Show Hide
Cp,gas 588.18 J/mol×K 722.73 Joback Calculated Property
Cp,gas 601.11 J/mol×K 758.09 Joback Calculated Property
Cp,gas 612.97 J/mol×K 793.46 Joback Calculated Property
Cp,gas 623.86 J/mol×K 828.82 Joback Calculated Property
Cp,gas 633.87 J/mol×K 864.19 Joback Calculated Property
Cp,gas 643.09 J/mol×K 899.55 Joback Calculated Property
Cp,gas 651.63 J/mol×K 934.92 Joback Calculated Property

Similar Compounds

Acetamide, n-(2,2,2-trifluoro-1,1-diphenylethyl)-. Acetamide, n-(1,1-bis(p-chlorophenyl)-2,2,2-trifluoroethyl)-. N-(1,1-Bis(4-chlorophenyl)-2,2,2-trichloroethyl)acetamide. 3-Carbomethoxyamino-3-phenyl-2,3-dihydrobenzofurane. D-Norleu, N-ethoxycarbonyl, (S)-1-phenylethylamide. L-Norleu, N-ethoxycarbonyl, (S)-1-phenylethylamide. L-«alpha»-Aminobutyric acid, N-ethoxycarbonyl, (S)-1-phenylethylamide. D-«alpha»-Aminobutyric acid, N-ethoxycarbonyl, (S)-1-phenylethylamide. Actinodaphnine. 3-Pentanoyloxymethylphenytoin. N-Acetylnornarcotine. Dimetindene M (nor, OH), acetylated. Cytosine arabinoside, methyl-TMS derivative. 2(1H)-Pyrimidinone, 1-[2,3-bis-O-(trimethylsilyl)-«beta»-D-ribofuranosyl]-4-(trimethylsiloxy)-, 5'-[bis(trimethylsilyl) phosphate]. Cytosine arabinoside, dimethyl-propyldimethylsilyl derivative.

Find more compounds similar to Acetamide, n-(2,2,2-trifluoro-1,1-bis(p-fluorophenyl)ethyl)-.

Sources

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