2-(2,4-DIFLUOROPHENYL)PYRIDINE

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CAS:391604-55-0
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CAS:391604-55-0
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Products Intro: Product Name:2-(2,4-difluorophenyl)pyridine
CAS:391604-55-0
Purity:98% Package:10MG;50MG;100MG,1G,5G,10G

2-(2,4-DIFLUOROPHENYL)PYRIDINE manufacturers

2-(2,4-DIFLUOROPHENYL)PYRIDINE Basic information
Product Name:2-(2,4-DIFLUOROPHENYL)PYRIDINE
Synonyms:2-(2,4-Difluorophenyl)pyridine;2-(2,4-Difluorophenyl)pyridine 97%;2-(2,4-Difluorophenyl)pyridine, min. 97%;2-(2,4-Difluorophenyl)pyridine>;Pyridine, 2-(2,4-difluorophenyl)-;2-(2,4-DIFLUOROPHENYL)PYRIDINE ISO 9001:2015 REACH;CAS:391604-55-0
CAS:391604-55-0
MF:C11H7F2N
MW:191.18
EINECS:
Product Categories:Fluorine series;API intermediates;OLED
Mol File:391604-55-0.mol
2-(2,4-DIFLUOROPHENYL)PYRIDINE Structure
2-(2,4-DIFLUOROPHENYL)PYRIDINE Chemical Properties
density 1.254 g/mL at 25 °C
refractive index n20/D1.570
Fp 103℃
storage temp. Inert atmosphere,Room Temperature
form crystal
pka3.91±0.25(Predicted)
color white
Boiling point 95°C/0.4 mmHg
InChI1S/C11H7F2N/c12-8-4-5-9(10(13)7-8)11-3-1-2-6-14-11/h1-7H
InChIKeySSABEFIRGJISFH-UHFFFAOYSA-N
SMILESFc1ccc(c(F)c1)-c2ccccn2
Safety Information
Hazard Codes Xn
Risk Statements 22-37/38-41-36/37/38
Safety Statements 26-39-24/25
WGK Germany 3
TSCA No
HS Code 29333990
Storage Class10 - Combustible liquids
Hazard ClassificationsAcute Tox. 4 Oral
Eye Dam. 1
Skin Irrit. 2
STOT SE 3
MSDS Information
2-(2,4-DIFLUOROPHENYL)PYRIDINE Usage And Synthesis
Chemical PropertiesColorless to dark yellow liquid
UsesLigand used in a blue-light emitting Ir(III) complexes suitable for use as phosphorescent OLEDs.
Synthesis
2-Bromopyridine

109-04-6

2,4-Difluorophenylboronic acid

144025-03-6

2-(2,4-DIFLUOROPHENYL)PYRIDINE

391604-55-0

General procedure for the synthesis of 2-(2,4-difluorophenyl)pyridine from 2-bromopyridine and 2,4-difluorophenylboronic acid: 2-bromopyridine (2.01 mL, 21.1 mmol), 2,4-difluorophenylboronic acid (4.00 g, 25.3 mmol), and tetrakis(triphenylphosphine)palladium(0) (0.732 g, 0.633 mmol) were added to a reflux condenser equipped with a round bottom flask and dissolved in 50 mL of tetrahydrofuran (THF). Subsequently, 30 mL of 2 M sodium carbonate (Na2CO3) aqueous solution was added to the reaction system. The reaction mixture was heated to reflux at 70°C for 24 hours. After completion of the reaction, it was cooled to room temperature and the crude reaction mixture was poured into water and extracted with dichloromethane (CH2Cl2, 50 mL x 3). The organic phases were combined and dried with anhydrous magnesium sulfate. Purification by silica gel column chromatography (eluent: n-hexane/ethyl acetate=4:1, v/v) afforded the target product 2-(2,4-difluorophenyl)pyridine (dfppy 1) as a colorless liquid (3.90 g, 97% yield).

References[1] Journal of the American Chemical Society, 2005, vol. 127, # 36, p. 12438 - 12439
[2] Inorganic Chemistry, 2017, vol. 56, # 19, p. 11565 - 11576
[3] Patent: US2012/273765, 2012, A1. Location in patent: Page/Page column 23-24
[4] Chemical Science, 2016, vol. 8, # 1, p. 348 - 360
[5] Patent: US2006/237715, 2006, A1. Location in patent: Page/Page column 11; 13
2-(2,4-DIFLUOROPHENYL)PYRIDINE Preparation Products And Raw materials
Raw materials2-Bromopyridine-->2-Chloropyridine-->2,4-Difluorophenylboronic acid-->Sodium carbonate-->Water-->Tetrahydrofuran
Tag:2-(2,4-DIFLUOROPHENYL)PYRIDINE(391604-55-0) Related Product Information
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