ChemicalBook--->CAS DataBase List--->115619-01-7

115619-01-7

115619-01-7 Structure

115619-01-7 Structure
IdentificationMore
[Name]

4-(4-Ethylpiperazin-1-ly)aniline
[CAS]

115619-01-7
[Synonyms]

4-(4-ETHYLPIPERAZIN-1-YL)ANILINE
4-(4-ETHYL-PIPERAZIN-1-YL)-PHENYLAMINE
4-(4-ETHYLPIPERAZINO)ANILINE
AKOS B021943
AKOS BB-8659
ART-CHEM-BB B021943
TIMTEC-BB SBB007132
4-(4-ETHYLPIPERAZIN-1-YL)PHENYLAMINE, 95+%
4-(4-Ethylpiperazin-1-ly)aniline
4-(4-ethylpiperazino)phenylamine
[Molecular Formula]

C12H19N3
[MDL Number]

MFCD00702246
[Molecular Weight]

205.3
[MOL File]

115619-01-7.mol
Chemical PropertiesBack Directory
[Melting point ]

76-78°C
[Boiling point ]

364.4±37.0 °C(Predicted)
[density ]

1.065±0.06 g/cm3(Predicted)
[storage temp. ]

Keep in dark place,Sealed in dry,2-8°C
[pka]

8.05±0.10(Predicted)
[Appearance]

Brown to black Solid
[CAS DataBase Reference]

115619-01-7(CAS DataBase Reference)
Safety DataBack Directory
[Symbol(GHS) ]

GHS hazard pictograms
GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319
[Precautionary statements ]

P264-P280-P302+P352-P337+P313-P305+P351+P338-P362+P364-P332+P313
[Hazard Codes ]

Xi
[RIDADR ]

3259
[HazardClass ]

IRRITANT
[PackingGroup ]

[HS Code ]

2933599590
Spectrum DetailBack Directory
[Spectrum Detail]

4-(4-Ethylpiperazin-1-ly)aniline(115619-01-7)1HNMR
Hazard InformationBack Directory
[Synthesis]

1-ETHYL-4-(4-NITROPHENYL)PIPERAZINE

115619-00-6

4-(4-Ethylpiperazin-1-ly)aniline

115619-01-7

General procedure: 1-ethyl-4-(4-nitrophenyl)piperazine (7.5 mmol) was dissolved in ethanol (50 mL) and 10% Pd/C catalyst (0.2 g) was added. The reaction mixture was stirred at room temperature and under hydrogen atmosphere for 9 hours. Upon completion of the reaction, the catalyst was removed by diatomaceous earth filtration. The filtrate was concentrated under high vacuum to give the target product 4-(4-ethyl-1-piperazinyl)aniline.

[References]

[1] Journal of Medicinal Chemistry, 2011, vol. 54, # 20, p. 7066 - 7083
[2] Bulletin of the Korean Chemical Society, 2015, vol. 36, # 7, p. 1863 - 1873
[3] Bioorganic and Medicinal Chemistry Letters, 2015, vol. 25, # 5, p. 1092 - 1099
[4] Patent: US2004/122237, 2004, A1. Location in patent: Page 180
[5] Patent: WO2006/420, 2006, A1. Location in patent: Page/Page column 210
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