ChemicalBook--->CAS DataBase List--->19675-63-9

19675-63-9

19675-63-9 Structure

19675-63-9 Structure
IdentificationMore
[Name]

4-CARBOXYCINNAMIC ACID
[CAS]

19675-63-9
[Synonyms]

3-(4-CARBOXYPHENYL)PROPENOIC ACID
4-(2-CARBOXYVINYL)BENZOIC ACID
4-CARBOXYCINNAMIC ACID
P-CARBOXYCINNAMIC ACID
RARECHEM BK HW 0113
4-Carboxycinnamic acid, predominantly trans, 98%
3-(4-Carboxyphenyl)acrylic acid
4-(2-Carboxyethenyl)benzoic acid
4-Carboxybenzeneacrylic acid
4-Carboxy-trans-cinnamic acid
[EINECS(EC#)]

243-220-4
[Molecular Formula]

C10H8O4
[MDL Number]

MFCD00016543
[Molecular Weight]

192.17
[MOL File]

19675-63-9.mol
Chemical PropertiesBack Directory
[Appearance]

cream fine powder
[Melting point ]

>300°C
[Boiling point ]

248.14°C (rough estimate)
[density ]

1.0825 (rough estimate)
[refractive index ]

1.4440 (estimate)
[storage temp. ]

Sealed in dry,Room Temperature
[form ]

powder
[pka]

4.12±0.10(Predicted)
[color ]

cream
[BRN ]

2614866
[CAS DataBase Reference]

19675-63-9(CAS DataBase Reference)
Safety DataBack Directory
[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 .
S36/37/39:Wear suitable protective clothing, gloves and eye/face protection .
[HS Code ]

2916399090
Hazard InformationBack Directory
[Chemical Properties]

cream fine powder
[Uses]

4-(2-Carboxyvinyl)benzoic Acid is used in preparation of Polycarboxylic Acid water reducer with good dispersion and slump resistance.
[Synthesis]

4-Iodobenzoic acid

619-58-9

Acrylic acid

79-10-7

4-CARBOXYCINNAMIC ACID

19675-63-9

In a typical reaction, 4-iodobenzoic acid (9 mmol), acrylic acid (15 mmol), tributylamine (30 mmol), and DMF (10 mL) were added to a round-bottomed flask containing 1.47 mol/L of AOFs-Ni(0) catalyst. The reaction was carried out in a temperature-controlled oil bath. After completion of the reaction, the mixture was cooled to room temperature. The AOFs-Ni(0) catalyst was separated from the mixture by filtration and washed sequentially with hot ethanol for next use. The filtrate was extracted with ethyl acetate (30 mL) and washed with distilled water (3 × 15 mL). Subsequently, the solvent was removed by rotary evaporation to give the crude product. The crude product was purified by column chromatography using mixed solvents (petroleum ether/ethyl acetate = 3/1) on H 60-silica powder. The purified 4-(2-carboxyvinyl)benzoic acid was characterized by melting point determination, 1H NMR, HRMS and GC-MS.

[References]

[1] RSC Advances, 2016, vol. 6, # 20, p. 16115 - 16121
[2] Applied Organometallic Chemistry, 2012, vol. 26, # 1, p. 16 - 20
[3] Journal of Chemical Research, 2016, vol. 40, # 3, p. 164 - 166
Spectrum DetailBack Directory
[Spectrum Detail]

4-CARBOXYCINNAMIC ACID(19675-63-9)1HNMR
Well-known Reagent Company Product InformationBack Directory
[Alfa Aesar]

4-Carboxycinnamic acid, predominantly trans, 98%(19675-63-9)
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