p-nitrophenol

CAS:
Other names:
SMILES: Oc1ccc(cc1)[N+]([O-])=O

Properties

MW HBA HBD LogP TPSA Rot. Comp. Fsp3C Brutto formula
139.11 2 1 1.82 66.05000000000001 1 34 0.00 C6H5NO3

Availability

Suppliers Supplier IDs Storage Storage ID Quantity Class Added
NT_c0201 None Jan. 1, 2023

Bar codes

Plate barcode Sample barcode

PAINS

Identified PAINS
Not checked

Supramolecules

Namelog KSDpHT(°C)MethodRef
[a-Cyclodextrin](1).[p-nitrophenol] 2.30 25.0 Potentiometric titration Kenneth A. Connors 1976
[a-Cyclodextrin](1).[p-nitrophenol] 2.46 25.0 Spectrophotometric method Kenneth A. Connors 1976
[a-Cyclodextrin](1).[p-nitrophenol] 2.24 3.0 30.0 NMR spectroscopy Soledad Penades 1993
[a-Cyclodextrin](1).[p-nitrophenol] 3.21 10.0 30.0 NMR spectroscopy Soledad Penades 1993
[a-Cyclodextrin](1).[p-nitrophenol] 3.20 7.4 23.0 UV-vis spectroscopy Jiri Horsky 1994
[a-Cyclodextrin](1).[p-nitrophenol] 2.22 0.05 7.0 30.0 NMR spectroscopy Yoshio Inoue 1992
[a-Cyclodextrin](1).[p-nitrophenol] 2.36 0.01 25.0 UV-vis spectroscopy Agustín G. Asuero 2006
[a-Cyclodextrin](1).[p-nitrophenol] 3.30 1.60 8.0 25.0 UV-vis spectroscopy Iwao Suzuki 2006
[a-Cyclodextrin](1).[p-nitrophenol] 2.18 0.48 3.0 25.0 UV and NMR spectroscopy Yoshihisa Matsui 1994
[a-Cyclodextrin](1).[p-nitrophenol] 2.16 0.70 3.5 25.0 UV and NMR spectroscopy Yoshihisa Matsui 1994
[a-Cyclodextrin](1).[p-nitrophenol] 2.17 0.30 4.0 25.0 UV and NMR spectroscopy Yoshihisa Matsui 1994
[a-Cyclodextrin](1).[p-nitrophenol] 3.27 1.38 10.0 25.0 UV and NMR spectroscopy Yoshihisa Matsui 1994
[a-Cyclodextrin](1).[p-nitrophenol] 3.27 1.30 10.4 25.0 UV and NMR spectroscopy Yoshihisa Matsui 1994
[a-Cyclodextrin](1).[p-nitrophenol] 3.27 1.30 11.0 25.0 UV and NMR spectroscopy Yoshihisa Matsui 1994
[a-Cyclodextrin](1).[p-nitrophenol] 3.38 2.48 11.0 25.0 capillary electrophoresis Daniel W. Armstrong 1996
[a-Cyclodextrin](1).[p-nitrophenol] 3.26 2.48 11.1 25.0 calorimetry Daniel W. Armstrong 1996
[a-Cyclodextrin](1).[p-nitrophenol] 3.36 11.0 25.0 UV spectroscopy Daniel W. Armstrong 1996
[a-Cyclodextrin](1).[p-nitrophenol] 2.83 10.0 25.0 NMR spectroscopy Daniel W. Armstrong 1996
[a-Cyclodextrin](1).[p-nitrophenol] 2.10 25.0 titration calorimetry Yannis L. Loukas 1997
[a-Cyclodextrin](1).[p-nitrophenol] 2.40 25.0 spectrophotometry Yannis L. Loukas 1997
[b-Cyclodextrin](1).[p-nitrophenol] 3.34 25.0 Potentiometric titration Kenneth A. Connors 1976
[b-Cyclodextrin](1).[p-nitrophenol] 3.35 25.0 Spectrophotometric method Kenneth A. Connors 1976
[b-Cyclodextrin](1).[p-nitrophenol] 2.41 3.0 30.0 NMR spectroscopy Soledad Penades 1993
[b-Cyclodextrin](1).[p-nitrophenol] 2.82 10.0 30.0 NMR spectroscopy Soledad Penades 1993
[b-Cyclodextrin](1).[p-nitrophenol] 2.70 7.4 23.0 UV-vis spectroscopy Jiri Horsky 1994
[b-Cyclodextrin](1).[p-nitrophenol] 2.27 7.0 30.0 NMR spectroscopy Yoshio Inoue 1992
[b-Cyclodextrin](1).[p-nitrophenol] 2.84 1.18 8.0 25.0 UV-vis spectroscopy Iwao Suzuki 2006
[b-Cyclodextrin](1).[p-nitrophenol] 2.42 5.0 25.0 Differential pulse polarography Carlos Bravo-Diaz 2002
[b-Cyclodextrin](1).[p-nitrophenol] 2.58 14.0 25.0 UV-vis spectroscopy Carlos Bravo-Diaz 2002
[b-Cyclodextrin](1).[p-nitrophenol] 2.89 10.0 25.0 Differential pulse polarography Carlos Bravo-Diaz 2002
[b-Cyclodextrin](1).[p-nitrophenol] 2.11 23.0 reverse-phase liquid chromatography (RPLC) Kazumi Fujimura 1986
[b-Cyclodextrin](1).[p-nitrophenol] 3.01 10.0 20.0 polarography Kazumi Fujimura 1986
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