Chemical Properties of Glutamine, N-trifluoroacetyl, 1-methylethyl ester

Glutamine, N-trifluoroacetyl, 1-methylethyl ester

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InChI
InChI=1S/C10H15F3N2O4/c1-5(2)19-8(17)6(3-4-7(14)16)15-9(18)10(11,12)13/h5-6H,3-4H2,1-2H3,(H2,14,16)(H,15,18)
InChI Key
IHJANNQLLFLEOG-UHFFFAOYSA-N
Formula
C10H15F3N2O4
SMILES
CC(C)OC(=O)C(CCC(N)=O)NC(=O)C(F)(F)F
Molecular Weight1
284.23
Sources

Physical Properties

Property Value Unit Source
Δf -889.07 kJ/mol Joback Calculated Property
Δfgas -1240.07 kJ/mol Joback Calculated Property
Δfus 32.72 kJ/mol Joback Calculated Property
Δvap 73.06 kJ/mol Joback Calculated Property
logPoct/wat 0.25 Crippen Calculated Property
Pc 2412.37 kPa Joback Calculated Property
Tboil 728.63 K Joback Calculated Property
Tc 920.58 K Joback Calculated Property
Tfus 484.59 K Joback Calculated Property
Vc 0.73 m3/kg-mol Joback Calculated Property

Temperature Dependent Properties

Property Value Unit Temperature (K) Source
Cp,gas 546.73 J/mol×K 728.63 Joback Calculated Property

Molecular Descriptors

Joback and Reid Groups
-O- (nonring) 1
>CH- 2
-F 3
>NH 1
-NH2 1
-CH2- 2
>C< 1
-CH3 2
>C=O (nonring) 3

Similar Compounds

ornithine, trifluoroacetyl-isopropyl ester. Norvaline, N-trifluoroacetyl, 1-methylethyl ester. Norleucine, N-trifluoroacetyl, 1-methylethyl ester. leucine, trifluoroacetyl-isopropyl ester. L-ornithine, n2,n5-bis(trifluoroacetyl)-, butyl ester. L-Glutamic acid, N-(trifluoroacetyl)-, dibutyl ester. L-Glutamine, N(«alpha»)-trifluoroacetyl-, 2,2,3,3,3-pentafluoropropyl ester. L-norleucine, n-(trifluoroacetyl)-, butyl ester. 2-Aminoadipic acid, n-trifluoroacetyl-, di-n-butyl ester. Glutamic anhydride, n-(trifluoroacetyl)-. Asparagine, N-trifluoroacetyl, 1-methylethyl ester. L-Glutamic acid, N-trifluoroacetyl-, bis(2,2,3,3,3-pentafluoropropyl) ester. L-valine, n-(trifluoroacetyl)-, butyl ester. L-Leucine, N-chlorodifluoroacetyl-, ethyl ester. L-methionine, n-(trifluoroacetyl)-, butyl ester.

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