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[3-[4-[[5-[(2,5-DIOXO-1-PYRROLIDINYL)-OXY]-1,5-DIOXOPENTYL]-AMINO]-PHENYL]-2-PHOSPHORYL-1-(4-NITROPHENYL)-PROPYL]-TRIMETHYL-AMMONIUM-IODIDE

Compound with spectra: 1 NMR

[3-[4-[[5-[(2,5-DIOXO-1-PYRROLIDINYL)-OXY]-1,5-DIOXOPENTYL]-AMINO]-PHENYL]-2-PHOSPHORYL-1-(4-NITROPHENYL)-PROPYL]-TRIMETHYL-AMMONIUM-IODIDE
SpectraBase Compound ID Fp9qUPpbkvh
InChI InChI=1S/C27H33N4O11P.HI/c1-31(2,3)27(19-9-13-21(14-10-19)30(36)37)22(42-43(38,39)40)17-18-7-11-20(12-8-18)28-23(32)5-4-6-26(35)41-29-24(33)15-16-25(29)34;/h7-14,22,27H,4-6,15-17H2,1-3H3,(H2-,28,32,38,39,40);1H/t22-,27-;/m0./s1
InChIKey UTHYCERRJZXRLO-QXWFTVPKSA-N
Mol Weight 748.5 g/mol
Molecular Formula C27H34IN4O11P
Exact Mass 748.10064 g/mol
Parent InChIKey ROSLOWHFNNNBBL-CUNXSJBXSA-N
Enantiomer InChIKey UTHYCERRJZXRLO-OHHMFLEWSA-N

View Spectrum of [3-[4-[[5-[(2,5-DIOXO-1-PYRROLIDINYL)-OXY]-1,5-DIOXOPENTYL]-AMINO]-PHENYL]-2-PHOSPHORYL-1-(4-NITROPHENYL)-PROPYL]-TRIMETHYL-AMMONIUM-IODIDE

31P NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CD3OD
3-[4-[[5-[(2,5-DIOXO-1-PYRROLIDINYL)-OXY]-1,5-DIOXOPENTYL]-AMINO]-PHENYL]-2-(O,O-DIMETHYLPHOSPHORYL)-1-(4-NITROPHENYL)-N,N-DIMETHYLPROPYLAMINE
N-Benzyloxycarbonyl-L-pyroglutamic acid N-succinimidyl ester
trans-3-Chloro-1-(p-methoxyphenyl)-4-(p-nitrophenyl)-2-azetidinone
5-METHYL-3-(4-NITROPHENYL)-2-PHENYL-ISOXAZOLIDINE-5-CARBALDEHYDE
SUCCINIMIDO-3-[METHOXY-(3,5,6-TRICHLOROPYRIDIN-2-YLOXY)-PHOSPHOROTHIOYLAMINO]-PROPANOATE
(4R*,6R*)-3,3,6-Trimethyl-4-p-methoxyphenyl-6-phenyltetrahydro-1,3-oxazinium dimethyl phosphate
3-chloro-4-(4-(dimethylamino)phenyl)-1-(4-(phenyldiaz-enyl)phenyl)azetidin-2-one
4-imidazolidinepropanamide, N-(4-butylphenyl)-2,5-dioxo-1-[(1S)-1-phenylethyl]-, (4S)-
4-[2-(6-methyl-1,2,4-triazin-5-yl)-1-(4-nitrophenyl)ethyl]-4-oxidanidyl-morpholin-4-ium
HDWCXOWSSWDMGD-MFCMXAAESA-N
Title Journal or Book Year
Esterolytic antibodies induced to haptens with a 1,2-amino alcohol functionality Journal of the American Chemical Society 1994
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