4-(4-Pyridinyl)benzaldehyde

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4-(4-Pyridinyl)benzaldehyde Basic information
Product Name:4-(4-Pyridinyl)benzaldehyde
Synonyms:AKOS BAR-0607;4-PYRIDIN-4-YL-BENZALDEHYDE;4-(4-PYRIDINYL)BENZALDEHYDE;4-(4-PYRIDYL)BENZALDEHYDE;4-(4-FORMYLPHENYL)PYRIDINE;4-(2-Chloropyridin-4-yl)benzaldehyde;4-(2-Fluoropyridin-4-yl)benzaldehyde;4-(3-Fluoropyridin-4-yl)benzaldehyde
CAS:99163-12-9
MF:C12H9NO
MW:183.21
EINECS:
Product Categories:
Mol File:99163-12-9.mol
4-(4-Pyridinyl)benzaldehyde Structure
4-(4-Pyridinyl)benzaldehyde Chemical Properties
Melting point 85-89 °C (lit.)
Boiling point 336.7±25.0 °C(Predicted)
density 1.147±0.06 g/cm3(Predicted)
storage temp. Keep in dark place,Inert atmosphere,Room temperature
form powder to crystal
pka4.98±0.10(Predicted)
color White to Orange to Green
InChIInChI=1S/C12H9NO/c14-9-10-1-3-11(4-2-10)12-5-7-13-8-6-12/h1-9H
InChIKeyMBJXDIYHLGBQOT-UHFFFAOYSA-N
SMILESC(=O)C1=CC=C(C2C=CN=CC=2)C=C1
CAS DataBase Reference99163-12-9(CAS DataBase Reference)
Safety Information
Hazard Codes Xn,Xi
Risk Statements 22-36/37/38
Safety Statements 26-36/37/39-22
WGK Germany 3
Hazard Note Irritant
HS Code 29333990
Storage Class11 - Combustible Solids
Hazard ClassificationsAcute Tox. 4 Oral
Eye Irrit. 2
Skin Irrit. 2
STOT SE 3
MSDS Information
ProviderLanguage
SigmaAldrich English
4-(4-Pyridinyl)benzaldehyde Usage And Synthesis
Chemical PropertiesWhite solid
Synthesis
Pyridine-4-boronic acid

1692-15-5

4-Bromobenzaldehyde

1122-91-4

4-(4-Pyridinyl)benzaldehyde

99163-12-9

Pyridine-4-boronic acid (498.3 mg, 4.05 mmol) and p-bromobenzaldehyde (500 mg, 2.70 mmol) were added to bis(triphenylporphyrinophosphate) palladium dichloride Pd(PPh3)2Cl2 (94.65 mg, 0.14 mmol) as a catalyst and dissolved in 20 mL of a solvent mixture of tetrahydrofuran and toluene (Vtoluene: VTHF = 1:1) in it. The reaction mixture was heated to 90°C under nitrogen protection for reflux reaction and the reaction process was monitored by thin layer chromatography (TLC). Upon completion of the reaction, the reaction solution was concentrated to remove the organic solvent and subsequently extracted with ethyl acetate. The organic layer was washed sequentially with water three times, saturated sodium chloride solution once, and then dried with anhydrous sodium sulfate. The dried organic phase was evaporated under reduced pressure to remove the solvent to obtain the crude product. The crude product was purified by silica gel column chromatography using a mixed solvent of petroleum ether and ethyl acetate (20:1) as eluent to finally obtain 4-(pyridin-4-yl)benzaldehyde (white solid, 288.7 mg, 68.4% yield).

References[1] Journal of the American Chemical Society, 2018, vol. 140, # 21, p. 6622 - 6630
[2] Journal of Medicinal Chemistry, 2018, vol. 61, # 18, p. 8402 - 8416
[3] Crystal Growth and Design, 2018, vol. 18, # 11, p. 6936 - 6945
[4] Patent: CN105418515, 2016, A. Location in patent: Paragraph 0087; 0088; 0089
[5] Angewandte Chemie - International Edition, 2006, vol. 45, # 17, p. 2761 - 2766
Tag:4-(4-Pyridinyl)benzaldehyde(99163-12-9) Related Product Information
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