128775
4-羟基哌啶
98%
别名:
4-哌啶醇
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选择尺寸
关于此项目
经验公式（希尔记法）:
C5H11NO
化学文摘社编号:
分子量:
101.15
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
226-373-1
Beilstein/REAXYS Number:
102738
MDL number:
产品名称
4-羟基哌啶, 98%
InChI key
HDOWRFHMPULYOA-UHFFFAOYSA-N
InChI
1S/C5H11NO/c7-5-1-3-6-4-2-5/h5-7H,1-4H2
SMILES string
OC1CCNCC1
assay
98%
bp
108-114 °C/10 mmHg (lit.)
functional group
hydroxyl
Quality Level
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Application
4-羟基哌啶（4-哌啶醇）可用于合成高效、高选择性的IP（PGI(2) 受体）激动剂。它也可用于研究铜催化的N-芳基化和O-芳基化作用。
General description
研究了4-羟基哌啶的分子结构、振动光谱、NBO和紫外光谱分析。已经发现具有取代的4-哌啶醇核心的化合物是人H（3）受体的有效拮抗剂。
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
S Sebastian et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 75(3), 941-952 (2010-01-09)
In this work, we report a combined experimental and theoretical study on molecular structure, vibrational spectra, NBO and UV-spectral analysis of 4-Hydroxypiperidine (4-HP). The FT-IR solid phase (4000-400 cm(-1)), FT-IR gas phase (5000-400 cm(-1)) and FT-Raman spectra (3500-50 cm(-1)) of
N- versus O-arylation of aminoalcohols: orthogonal selectivity in copper-based catalysts.
Alexandr Shafir et al.
Journal of the American Chemical Society, 129(12), 3490-3491 (2007-03-08)
James T Anderson et al.
Bioorganic & medicinal chemistry letters, 20(21), 6246-6249 (2010-09-14)
Compounds containing a substituted 4-piperidinol core have been found to be potent antagonists of the human H(3) receptor. The compounds exhibited up to a 60-fold preference for inhibiting the human H(3) receptor over the mouse and showed a low binding
Yasuhiro Morita et al.
Molecules (Basel, Switzerland), 17(2), 1233-1246 (2012-02-02)
An efficient synthesis of a highly potent and selective IP (PGI(2) receptor) agonist that is not structurally analogous to PGI(2) is described. This synthesis is accomplished through the following key steps: Nucleophilic ring-opening of 3-(4-chlorophenyl)-oxazolidin-2-one prepared by a one-pot procedure
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