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Thermo Scientific Chemicals
4-Acetylpyridine, 98%
CAS: 1122-54-9 | C7H7NO | 121.139 g/mol
化学物質識別子
CAS1122-54-9
IUPAC Name1-(pyridin-4-yl)ethan-1-one
Molecular FormulaC7H7NO
InChI KeyWMQUKDQWMMOHSA-UHFFFAOYSA-N
SMILESCC(=O)C1=CC=NC=C1
さらに表示
仕様
スペックシート
スペックシートAppearance (Color)Clear colorless to yellow
FormLiquid
Assay (GC)≥97.5%
Refractive Index1.5275-1.5315 @ 20?C
4-acetylpyridine on reaction with - and 4-formylpyridine (H3FoPyS, H4FoPyS) yields semicarbazones. Reaction of acetylpyridine with thiophene-2-carboxaldehyde afforded the 2-chloro-6-ethoxy-4-β-(2-thienyl)acryloylpyridine, which was reacted with malononitrile in refluxing ethanol in the presence of piperidine as a catalyst to afford the cyanoaminopyrane derivative.
This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.
Applications
4-acetylpyridine on reaction with - and 4-formylpyridine (H3FoPyS, H4FoPyS) yields semicarbazones. Reaction of acetylpyridine with thiophene-2-carboxaldehyde afforded the 2-chloro-6-ethoxy-4-β-(2-thienyl)acryloylpyridine, which was reacted with malononitrile in refluxing ethanol in the presence of piperidine as a catalyst to afford the cyanoaminopyrane derivative.
Solubility
Insoluble in water. Soluble in alcohol.
Notes
Store in cool place. Keep away from oxidizing agents.
4-acetylpyridine on reaction with - and 4-formylpyridine (H3FoPyS, H4FoPyS) yields semicarbazones. Reaction of acetylpyridine with thiophene-2-carboxaldehyde afforded the 2-chloro-6-ethoxy-4-β-(2-thienyl)acryloylpyridine, which was reacted with malononitrile in refluxing ethanol in the presence of piperidine as a catalyst to afford the cyanoaminopyrane derivative.
Solubility
Insoluble in water. Soluble in alcohol.
Notes
Store in cool place. Keep away from oxidizing agents.
RUO – Research Use Only
General References:
- I.C. Mendesa.; L.R. Teixeira.; R. Limaa.; H. Beraldo.; N.L. Spezialib, D.X. West. Structural and spectral studies of thiosemicarbazones derived from 3- and 4-formylpyridine and 3- and 4-acetylpyridine. Journal of Molecular Structure. 2001, 559 (1-3),355-360.
- Michael W. George.; Martyn Poliakoff .; James J. Turner. Nanosecond time-resolved infrared spectroscopy: a comparative view of spectrometers and their applications in organometallic chemistry. Analyst. 1994, 119 (4), 551-560.