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128775

4-羟基哌啶

Name: 4-羟基哌啶
Brand: ALDRICH

98%

别名:

4-哌啶醇

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关于此项目

经验公式（希尔记法）:

C₅H₁₁NO

化学文摘社编号:

5382-16-1

分子量:

101.15

UNSPSC Code:

12352100

NACRES:

NA.22

PubChem Substance ID:

24847875

EC Number:

226-373-1

Beilstein/REAXYS Number:

102738

MDL number:

MFCD00005999

Assay:

98%

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属性

Quality Level

200

assay

98%

bp

108-114 °C/10 mmHg (lit.)

functional group

hydroxyl

SMILES string

OC1CCNCC1

InChI

1S/C5H11NO/c7-5-1-3-6-4-2-5/h5-7H,1-4H2

InChI key

HDOWRFHMPULYOA-UHFFFAOYSA-N

说明

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。

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。

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pictograms

GHS07

signalword

Warning

hcodes

H315,H319

pcodes

P264 - P280 - P302 + P352 - P305 + P351 + P338 - P332 + P313 - P337 + P313

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

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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The spectroscopic (FT-IR, FT-IR gas phase, FT-Raman and UV) and NBO analysis of 4-Hydroxypiperidine by density functional method.

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)

Investigation of 4-piperidinols as novel H3 antagonists.

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

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128775-5G	04061833320167
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128775-100G	04061838345707