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ChemicalBook > Product Catalog >Pharmaceutical intermediates >Heterocyclic compound >Pyridine compound >Pyridine derivatives >1-(2-CHLORO-PYRIDIN-4-YL)-ETHANONE

1-(2-CHLORO-PYRIDIN-4-YL)-ETHANONE

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Products Intro: CAS:23794-15-2
Purity:98% HPLC Package:5G;10G;25G;50G;100G;250G;1KG
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Products Intro: Product Name:1-(2-chloropyridine-4-yl)ethanone
CAS:23794-15-2
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Products Intro: Product Name:1-(2-chloropyridin-4-yl)ethanone
CAS:23794-15-2
Purity:99% Package:1kg

1-(2-CHLORO-PYRIDIN-4-YL)-ETHANONE manufacturers

1-(2-CHLORO-PYRIDIN-4-YL)-ETHANONE Basic information
Product Name:1-(2-CHLORO-PYRIDIN-4-YL)-ETHANONE
Synonyms:1-(2-chloro-4-pyridinyl)ethanone(SALTDATA: FREE);Ethanone, 1-(2-chloro-4-pyridinyl)-;1-(2-Chloro-4-pyridinyl)ethanone;1-(2-Chloro-4-pyridyl)ethanone;4-ACETYL-2-CHLOROPYRIDINE;1-(2-CHLORO-PYRIDIN-4-YL)-ETHANONE;1-(2-chloro-4-pyridinyl)-1-ethanone;1-(2-chloropyridine-4-yl)ethanone
CAS:23794-15-2
MF:C7H6ClNO
MW:155.58
EINECS:
Product Categories:Pyridines;Pyridine series
Mol File:23794-15-2.mol
1-(2-CHLORO-PYRIDIN-4-YL)-ETHANONE Structure
1-(2-CHLORO-PYRIDIN-4-YL)-ETHANONE Chemical Properties
Melting point 36.5 °C
Boiling point 270.2±25.0 °C(Predicted)
density 1.233±0.06 g/cm3(Predicted)
Fp >110℃
storage temp. Keep in dark place,Sealed in dry,Room Temperature
pka-1.55±0.10(Predicted)
form solid
color Off white to brown
Safety Information
Hazard Codes Xi
Risk Statements 36/37/38
Safety Statements 26-36
RIDADR UN2811
WGK Germany 3
Hazard Note Harmful
HazardClass IRRITANT-HARMFUL
HazardClass 6.1
HS Code 2933399990
MSDS Information
1-(2-CHLORO-PYRIDIN-4-YL)-ETHANONE Usage And Synthesis
Uses1-(2-Chloro-4-pyridinyl)ethanone is used for the synthesis of pyrimidine derivatives as hSMG-1 inhibitors in the treatment of cancer.
Synthesis
2-Chloro-N-methoxy-N-methylisonicotinamide

250263-39-9

Methylmagnesium Bromide

75-16-1

1-(2-CHLORO-PYRIDIN-4-YL)-ETHANONE

23794-15-2

Step 2: Synthesis of 1-(2-chloropyridin-4-yl)ethanone To a solution of 2-chloro-N-methoxy-N-methylisonicotinamide (10.0 g, 50 mmol) in anhydrous tetrahydrofuran (50 mL) was slowly added 3M methylmagnesium bromide solution in tetrahydrofuran (50 mL, 150 mmol) at 0 °C, keeping stirring. After addition, the reaction mixture was gradually warmed to room temperature and stirring was continued overnight. Upon completion of the reaction, the reaction was quenched with saturated aqueous ammonium chloride solution, followed by extraction of the organic phase with ethyl acetate. The organic layers were combined, dried over anhydrous sodium sulfate, filtered and concentrated under reduced pressure. The crude product was purified by silica gel column chromatography to afford 1-(2-chloropyridin-4-yl)ethanone (7.5 g, 96% yield). Mass spectrometric analysis (ESI) showed m/z: 156.0 [M + H]+.

References[1] Patent: EP2952510, 2015, A1. Location in patent: Paragraph 0106
[2] Bioorganic and Medicinal Chemistry Letters, 2012, vol. 22, # 21, p. 6636 - 6641,6
[3] Patent: WO2016/97351, 2016, A1. Location in patent: Page/Page column 11-12
[4] Patent: WO2004/78682, 2004, A2. Location in patent: Page 17-18
[5] Patent: US2012/225876, 2012, A1. Location in patent: Page/Page column 50
Tag:1-(2-CHLORO-PYRIDIN-4-YL)-ETHANONE(23794-15-2) Related Product Information
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