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Merck
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119725

Sigma-Aldrich

4-哌啶苯乙酮

97%

别名:

1-[4-(1-Piperidinyl)]phenyl]ethanone

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About This Item

经验公式（希尔记法）:
C13H17NO
CAS号:
10342-85-5
分子量:
203.28
EC號碼:
233-746-2
MDL號碼:
MFCD00006481
分類程式碼代碼:
12352100
PubChem物質ID:
24847298
NACRES:
NA.22

化驗

97%

mp

85-87 °C (lit.)

官能基

ketone

SMILES 字串

CC(=O)c1ccc(cc1)N2CCCCC2

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

InChI 密鑰

JCMZZYSPSGHBNM-UHFFFAOYSA-N

一般說明

4′-Piperidinoacetophenone undergoes Claisen-Schmidt condensation with substituted benzaldehydes using NaOH-Al2O3 by microwave irradiation to give chalcones. It has antimycobacterial activity.

應用

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

象形圖

Exclamation mark
GHS07

訊號詞

Warning

危險聲明

H315,H319,H335

危險分類

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

標靶器官

Respiratory system

儲存類別代碼

11 - Combustible Solids

水污染物質分類（WGK）

WGK 3

閃點（°F）

Not applicable

閃點（°C）

Not applicable

個人防護裝備

dust mask type N95 (US), Eyeshields, Gloves

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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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