Chemical Properties of L-Pipecolic acid, N-ethoxycarbonyl, (S)-1-phenylethylamide

L-Pipecolic acid, N-ethoxycarbonyl, (S)-1-phenylethylamide

Download as PDF file Download as Excel file Download as 2D mole file Predict properties

InChI
InChI=1S/C17H24N2O3/c1-3-22-17(21)19-12-8-7-11-15(19)16(20)18-13(2)14-9-5-4-6-10-14/h4-6,9-10,13,15H,3,7-8,11-12H2,1-2H3,(H,18,20)/t13-,15+/m0/s1
InChI Key
ZIMZRTQSTJRFHY-DZGCQCFKSA-N
Formula
C17H24N2O3
SMILES
CCOC(=O)N1CCCCC1C(=O)NC(C)c1ccccc1
Molecular Weight1
304.38
Sources

Physical Properties

Property Value Unit Source
logPoct/wat 2.87 Crippen Calculated Property

Similar Compounds

D-Pipecolic acid, N-ethoxycarbonyl, (S)-1-phenylethylamide. L-Pro, N-ethoxycarbonyl, (S)-1-phenylethylamide. D-Pro, N-ethoxycarbonyl, (S)-1-phenylethylamide. L-Norleu, N-ethoxycarbonyl, (S)-1-phenylethylamide. D-Norleu, N-ethoxycarbonyl, (S)-1-phenylethylamide. D-Aspartic acid, N-methyl, N-ethoxycarbonyl, (S)-1-phenylethylamide. L-Aspartic acid, N-methyl, N-ethoxycarbonyl, (S)-1-phenylethylamide. D-Norval, N-ethoxycarbonyl, (S)-1-phenylethylamide. L-Norval, N-ethoxycarbonyl, (S)-1-phenylethylamide. L-Leu, N-ethoxycarbonyl, (S)-1-phenylethylamide. D-Leu, N-ethoxycarbonyl, (S)-1-phenylethylamide. L-Ile, N-ethoxycarbonyl, (S)-1-phenylethylamide. D-Ile, N-ethoxycarbonyl, (S)-1-phenylethylamide. L-«alpha»-Aminobutyric acid, N-ethoxycarbonyl, (S)-1-phenylethylamide. D-«alpha»-Aminobutyric acid, N-ethoxycarbonyl, (S)-1-phenylethylamide.

Find more compounds similar to L-Pipecolic acid, N-ethoxycarbonyl, (S)-1-phenylethylamide.

Note: Cheméo is only indexing the data, follow the source links to retrieve the latest data. The source is also providing more information like the publication year, authors and more. Take the time to validate and double check the source of the data.