119725
4-哌啶苯乙酮
97%
别名:
1-[4-(1-Piperidinyl)]phenyl]ethanone
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关于此项目
经验公式（希尔记法）:
C13H17NO
化学文摘社编号:
分子量:
203.28
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
233-746-2
MDL number:
Assay:
97%
InChI key
JCMZZYSPSGHBNM-UHFFFAOYSA-N
InChI
1S/C13H17NO/c1-11(15)12-5-7-13(8-6-12)14-9-3-2-4-10-14/h5-8H,2-4,9-10H2,1H3
SMILES string
CC(=O)c1ccc(cc1)N2CCCCC2
assay
97%
mp
85-87 °C (lit.)
functional group
ketone
General description
4′-Piperidinoacetophenone undergoes Claisen-Schmidt condensation with substituted benzaldehydes using NaOH-Al2O3 by microwave irradiation to give chalcones. It has antimycobacterial activity.
Application
4′-Piperidinoacetophenone was used as internal standard in the determination of pethidine, a narcotic analgesic drug in body fluids by gas chromatography-tandem mass spectrometry.
Pharmacological activity:
- Selective antimycobacterial activity
- Bronchodilator compound
- Modulation of flagellar motility in Chlamydomonas
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
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
法规信息
新产品
此项目有
Akira Ishii et al.
Journal of chromatography. B, Analytical technologies in the biomedical and life sciences, 792(1), 117-121 (2003-06-28)
We have presented a simple and sensitive method for determining pethidine, a narcotic analgesic drug in body fluids by gas chromatography-tandem mass spectrometry (GC-MS/MS). Pethidine and 4'-piperidinoacetophenone (internal standard) were extracted from body fluids with Bond Elut C(18) columns; the
Microwave enhanced Claisen-Schmidt condensation: A green route to chalcones.
Singh JP, et al.
Indian J. Chem. B, 51(11), 1623-1623 (2012)
L Rajabi et al.
Letters in applied microbiology, 40(3), 212-217 (2005-02-18)
Mycobacteria are a serious cause of infections in humans, with limited treatment options, as no new antibiotics have been developed against mycobacteria since the 1960s. In this study, the antimycobacterial activity of a small library of acetophenone (AP) compounds was
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