Chemical Properties of Niacinamide, N-heptafluorobutyryl-

Niacinamide, N-heptafluorobutyryl-

InChI
InChI=1S/C10H5F7N2O2/c11-8(12,9(13,14)10(15,16)17)7(21)19-6(20)5-2-1-3-18-4-5/h1-4H,(H,19,20,21)
InChI Key
AQGBZAXSFMDMIA-UHFFFAOYSA-N
Formula
C10H5F7N2O2
SMILES
O=C(NC(=O)C(F)(F)C(F)(F)C(F)(F)F)c1cccnc1
Molecular Weight1
318.15
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Physical Properties

Property Value Unit Source
Δfgas -1694.85 kJ/mol Relay (1.0) Calculated Property
Δvap 76.12 kJ/mol Relay (1.0) Calculated Property
IE 10.21 eV Relay (1.0) Calculated Property
log10WS -3.56 Relay (1.0) Calculated Property
logPoct/wat 2.171 Crippen Calculated Property
McVol 163.490 ml/mol McGowan Calculated Property
Inp [1847.00; 1847.00]   Show Hide
Inp 1847.00 NIST
Inp 1847.00 NIST
Tboil 519.03 K Relay (1.0) Calculated Property
Tfus 358.48 K Relay (1.0) Calculated Property

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Similar Compounds

Niacinamide, N-pentafluoropropionyl-. Niacinamide, N-trifluoroacetyl-. Aucubin, hexakis(trimethylsilyl) ether. N-ACETYLCOLCHINOL METHYL ETHER. Dimetindene M (nor, OH), acetylated. L-Alanine, N-[N-[N-[N-(1-oxodecyl)glycyl]-L-tryptophyl]-L-alanyl]-, methyl ester. Colchicine, (+)-. Colchicine. Colchicine. Oxazolam. Tryptophan, N-acetyl-5-methoxy, TMS. Thymidine, 3'-O-acetyl, 5'-O-TBDMS. inosine-5'-monophosphate, TMS. 3'-Deoxyguanosine, tris(trimethylsilyl) deriv.. Oxycodone, trimethylsilyl ether.

Find more compounds similar to Niacinamide, N-heptafluorobutyryl-.

Sources

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