ChemicalBook--->CAS DataBase List--->17071-24-8

17071-24-8

17071-24-8 Structure

17071-24-8 Structure
IdentificationBack Directory
[Name]

Ethanone, 1-(3-amino-4-methylphenyl)- (9CI)
[CAS]

17071-24-8
[Synonyms]

1-(3-amino-4-methyl-phenyl)ethanone
1-(3-amino-4-methylphenyl)ethan-1-one
Ethanone, 1-(3-amino-4-methylphenyl)-
Ethanone, 1-(3-amino-4-methylphenyl)- (9CI)
1-(3-amino-4-methylphenyl)ethanone(SALTDATA: FREE)
[Molecular Formula]

C9H11NO
[MOL File]

17071-24-8.mol
[Molecular Weight]

149.19
Chemical PropertiesBack Directory
[Melting point ]

83 °C
[Boiling point ]

306.4±22.0 °C(Predicted)
[density ]

1.069±0.06 g/cm3(Predicted)
[storage temp. ]

Keep in dark place,Inert atmosphere,2-8°C
[form ]

solid
[pka]

3.27±0.10(Predicted)
[Appearance]

Off-white to yellow Solid
Safety DataBack Directory
[HS Code ]

2922390090
Spectrum DetailBack Directory
[Spectrum Detail]

Ethanone, 1-(3-amino-4-methylphenyl)- (9CI)(17071-24-8)1HNMR
Hazard InformationBack Directory
[Synthesis]

4-Methyl-3-nitroacetophenone

5333-27-7

Ethanone, 1-(3-amino-4-methylphenyl)- (9CI)

17071-24-8

General procedure for the synthesis of 3-amino-4-methylacetophenone from 3-nitro-4-methylacetophenone: 5% palladium-carbon catalyst (wet state, 100 mg) was added to a solution of ethanol (12 mL) containing 3-nitro-4-methylacetophenone (0.4 g, 2.23 mmol). The reaction flask was evacuated and displaced with hydrogen (repeated three times). After stirring the reaction mixture under hydrogen atmosphere for 3 hours, the catalyst was removed by filtration and the filtrate was concentrated to give 3-amino-4-methylacetophenone (330 mg, 99% yield).

[References]

[1] Patent: WO2003/90912, 2003, A1. Location in patent: Page/Page column 129
[2] Helvetica Chimica Acta, 2010, vol. 93, # 7, p. 1261 - 1273
[3] ACS Medicinal Chemistry Letters, 2018, vol. 9, # 8, p. 854 - 859
[4] ACS Medicinal Chemistry Letters, 2015, vol. 6, # 7, p. 798 - 803
[5] Patent: CN105481790, 2016, A. Location in patent: Paragraph 0130; 0131; 0132; 0133
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