ChemicalBook--->CAS DataBase List--->5048-82-8

5048-82-8

5048-82-8 Structure

5048-82-8 Structure
IdentificationMore
[Name]

Ethyl 4-aminocinnamate
[CAS]

5048-82-8
[Synonyms]

2-PROPENOIC ACID, 3-(4-AMINOPHENYL)-, ETHYL ESTER
3-(4-AMINO-PHENYL)-ACRYLIC ACID ETHYL ESTER
4-AMINOCINNAMIC ACID ETHYL ESTER
4-AMINOETHYLCINNAMATE
ETHYL (2E)-3-(4-AMINOPHENYL)ACRYLATE
ETHYL 4-AMINOCINNAMATE
ETHYL P-AMINOCINNAMATE
TRANS-3-(4-AMINOPHENYL)ACRYLATE ETHYL ESTER
3-(4-aminophenyl)-2-propenoicaciethylester
Cinnamic acid, p-amino-, ethyl ester
Ethyl (2E)-3-(4-aminophenyl)-2-propenoate
Ethyl4-aminocinnamate,97%
ACRYLICACID,PHENYLAMINOETHYLESTER
3-(4-aminophenyl)-2-propenoic acid ethyl ester
3-(4-Aminophenyl)propenoic acid ethyl ester
4-Aminobenzeneacrylic acid ethyl ester
[EINECS(EC#)]

225-747-1
[Molecular Formula]

C11H13NO2
[MDL Number]

MFCD00017116
[Molecular Weight]

191.23
[MOL File]

5048-82-8.mol
Chemical PropertiesBack Directory
[Melting point ]

70-74 °C (lit.)
[Boiling point ]

347.0±25.0 °C(Predicted)
[density ]

1.130±0.06 g/cm3(Predicted)
[storage temp. ]

under inert gas (nitrogen or Argon) at 2–8 °C
[form ]

solid
[pka]

2.89±0.10(Predicted)
[Appearance]

Yellow to orange Solid
[BRN ]

2803541
[InChI]

1S/C11H13NO2/c1-2-14-11(13)8-5-9-3-6-10(12)7-4-9/h3-8H,2,12H2,1H3/b8-5+
[InChIKey]

NRPMBSHHBFFYBF-VMPITWQZSA-N
[SMILES]

[H]\C(=C(\[H])c1ccc(N)cc1)C(=O)OCC
[CAS DataBase Reference]

5048-82-8(CAS DataBase Reference)
[NIST Chemistry Reference]

Ethyl p-aminocinnamate(5048-82-8)
[EPA Substance Registry System]

5048-82-8(EPA Substance)
Safety DataBack Directory
[Hazard Codes ]

Xi
[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 .
[WGK Germany ]

3
[Hazard Note ]

Irritant
[TSCA ]

Yes
[HS Code ]

29163990
[Storage Class]

11 - Combustible Solids
[Hazard Classifications]

Eye Irrit. 2
Skin Irrit. 2
STOT SE 3
Spectrum DetailBack Directory
[Spectrum Detail]

Ethyl 4-aminocinnamate(5048-82-8)1HNMR
Well-known Reagent Company Product InformationBack Directory
[Alfa Aesar]

Ethyl 4-aminocinnamate, 97%(5048-82-8)
[Sigma Aldrich]

5048-82-8(sigmaaldrich)
Hazard InformationBack Directory
[Synthesis]

ETHYL (2E)-3-(4-NITROPHENYL)ACRYLATE

24393-61-1

Ethyl 4-aminocinnamate

5048-82-8

General procedure for the synthesis of ethyl 4-aminocinnamate from ethyl (E)-3-(4-nitrophenyl)acrylate: to an 8 mL glass vial (14 mm diameter, 50 mm height) equipped with a PTFE-coated oval magnetic stirring bar (8.5 mm) and a plastic screw cap was added ethyl (E)-3-(4-nitrophenyl)acrylate (0.5 mmol, 1.0 equivalents), Fe2O3/NGr(at)C catalyst (50 mg, 4.0 mol% Fe), triethylamine (Et3N, 70 μL, 0.5 mmol, 1.0 equivalents), tetrahydrofuran (THF, 2 mL) and deionized water (H2O, 0.2 mL). The silicone septum was punctured with a 26-gauge syringe needle (0.45 × 12 mm), and the vial was placed in an aluminum plate and transferred to a 300-mL autoclave. After sealing the autoclave, it was placed in an aluminum block and purged with carbon monoxide (CO, 5-10 bar) three times. This was followed by pressurization with CO to 30 bar and addition of nitrogen (N2) at 20 bar. The aluminum block was heated to 125°C with sufficient stirring (700 rpm). After 24 hours of reaction, the autoclave was removed from the aluminum block and cooled to room temperature. After releasing the remaining gas in a water bath, the vial containing the reaction mixture was removed. The reaction mixture was filtered through a diatomaceous earth pad (about 1 cm thick), the filtrate was concentrated and finally analyzed by gas chromatography (GC) and nuclear magnetic resonance (NMR) spectroscopy (Table 2).

[References]

[1] Advanced Synthesis and Catalysis, 2012, vol. 354, # 2-3, p. 321 - 327
[2] Synthesis (Germany), 2018, vol. 50, # 22, p. 4369 - 4376
[3] Journal of Organic Chemistry, 1999, vol. 64, # 7, p. 2301 - 2303
[4] Organic Letters, 2017, vol. 19, # 24, p. 6518 - 6521
[5] Journal of Medicinal Chemistry, 2016, vol. 59, # 19, p. 8967 - 9004
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