ChemicalBook--->CAS DataBase List--->84228-93-3

84228-93-3

84228-93-3 Structure

84228-93-3 Structure
IdentificationMore
[Name]

3-(4-Pyridine)acrylic acid
[CAS]

84228-93-3
[Synonyms]

(2E)-3-PYRIDIN-4-YLACRYLIC ACID
3-(4-PYRIDINYL)ACRYLIC ACID
3-(4-PYRIDYL)ACRYLIC ACID
3-(PYRID-4-YL)ACRYLIC ACID
3-PYRIDIN-4-YL-ACRYLIC ACID
B-(4-PYRIDYL)-ACRYLIC ACID
IFLAB-BB F2124-0554
RARECHEM AH CK 0189
TRANS-3-(4-PYRIDYL)ACRYLIC ACID
3-(4-Pyridine)acrylic acid
[EINECS(EC#)]

226-265-4
[Molecular Formula]

C8H7NO2
[MDL Number]

MFCD00040746
[Molecular Weight]

149.15
[MOL File]

84228-93-3.mol
Chemical PropertiesBack Directory
[Melting point ]

276-280°C
[Boiling point ]

317.5±17.0 °C(Predicted)
[density ]

1.261±0.06 g/cm3(Predicted)
[storage temp. ]

Inert atmosphere,Room Temperature
[pka]

3.13±0.10(Predicted)
[Appearance]

White to off-white Solid
[BRN ]

1719967
[CAS DataBase Reference]

84228-93-3(CAS DataBase Reference)
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319-H335
[Precautionary statements ]

P261-P280a-P304+P340-P305+P351+P338-P405-P501a
[Risk Statements ]

R36/37/38:Irritating to eyes, respiratory system and skin .
[Safety Statements ]

S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
S36:Wear suitable protective clothing .
Spectrum DetailBack Directory
[Spectrum Detail]

3-(4-Pyridine)acrylic acid(84228-93-3)1HNMR
Well-known Reagent Company Product InformationBack Directory
[Alfa Aesar]

trans-3-(4-Pyridyl)acrylic acid, 97%(84228-93-3)
Hazard InformationBack Directory
[Synthesis]

Piperidine

110-89-4

4-Pyridinecarboxaldehyde

872-85-5

3-(4-Pyridine)acrylic acid

84228-93-3

A. Preparation of (E)-3-(pyridin-4-yl)acrylic acid 4-Pyridinecarboxaldehyde (18.96 g, 0.177 mol) and malonic acid (55.3 g, 0.53 mol) were dissolved in 200 mL of pyridine. Piperidine (5.25 mL, 0.053 mol) was added to the solution and the reaction mixture was subsequently heated to reflux for 6 hours. After completion of the reaction, the mixture was cooled in an ice bath and the precipitated white solid was separated by filtration and washed with ether and dried to give 20.1 g of (E)-3-(pyridin-4-yl)acrylic acid. The filtrate was further concentrated, filtered again and washed with aqueous ethyl ether to afford an additional 2.2 g of product in a total yield of 84%.

[References]

[1] Patent: EP846687, 1998, A1
[2] Patent: US5972972, 1999, A
[3] Patent: US5618939, 1997, A
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