2-(4-AMINOPHENYL)-2-METHYLPROPANENITRILE

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Products Intro: Product Name:2-(4-aminophenyl)-2-methylpropanenitrile
CAS:115279-57-7
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Products Intro: Product Name:2-(4-AMinophenyl)-2-Methylpropanenitrile
CAS:115279-57-7
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2-(4-AMINOPHENYL)-2-METHYLPROPANENITRILE manufacturers

2-(4-AMINOPHENYL)-2-METHYLPROPANENITRILE Basic information
Uses
Product Name:2-(4-AMINOPHENYL)-2-METHYLPROPANENITRILE
Synonyms:2-(4-AMINOPHENYL)-2-METHYLPROPANENITRILE;2-(4-Aminophenyl)-2-methylpropionitrile;1,1-dimethyl-1-(4-aminophenyl)-acetonitrile;Benzeneacetonitrile, 4-aMino-a,a-diMethyl-;Benzeneacetonitrile, 4-amino-α,α-dimethyl-;2-(4-AMINOPHENYL)-2-METHYLPROPANENITRILE ISO 9001:2015 REACH;"4-Amino-α, α-dimethylbenzeneacetonitrile 13C6";13C6]-4-Amino-α, α-dimethylbenzeneacetonitrile
CAS:115279-57-7
MF:C10H12N2
MW:160.22
EINECS:
Product Categories:
Mol File:115279-57-7.mol
2-(4-AMINOPHENYL)-2-METHYLPROPANENITRILE Structure
2-(4-AMINOPHENYL)-2-METHYLPROPANENITRILE Chemical Properties
Boiling point 173-174 °C(Press: 10 Torr)
density 1.055±0.06 g/cm3(Predicted)
storage temp. under inert gas (nitrogen or Argon) at 2–8 °C
pka3.63±0.10(Predicted)
AppearanceLight brown to off-white Solid
InChIInChI=1S/C10H12N2/c1-10(2,7-11)8-3-5-9(12)6-4-8/h3-6H,12H2,1-2H3
InChIKeyVXDPOGVDHHJTDY-UHFFFAOYSA-N
SMILESCC(C1=CC=C(N)C=C1)(C)C#N
Safety Information
HS Code 2926907090
MSDS Information
2-(4-AMINOPHENYL)-2-METHYLPROPANENITRILE Usage And Synthesis
Uses2-(4-Aminophenyl)-2-methylpropionitrile is used as an organic and pharmaceutical intermediate.
Chemical Propertieslight yellow crystalline
Synthesis
2-methyl-2-(4-nitrophenyl)propanenitrile

71825-51-9

2-(4-AMINOPHENYL)-2-METHYLPROPANENITRILE

115279-57-7

General procedure for the synthesis of 2-(4-aminophenyl)-2-methylpropionitrile from 2-methyl-2-(4-nitrophenyl)propanenitrile: 2-methyl-2-(4-nitrophenyl)propanenitrile (1.0 mmol) was dissolved in ethyl acetate (20 mL) and stannous chloride dihydrate (3.52 g, 15.86 mmol) was added. The reaction mixture was stirred at room temperature overnight. Upon completion of the reaction, the reaction mixture was alkalized with aqueous sodium carbonate. The organic layer was separated, washed with water, dried over anhydrous sodium sulfate and concentrated under reduced pressure to give the crude product. The crude product was purified by silica gel column chromatography with the eluent of ethyl acetate/petroleum ether (1:9, v/v) to afford 2-(4-aminophenyl)-2-methylpropanenitrile (0.45 g, 89% yield) as an oil.

References[1] Journal of Medicinal Chemistry, 2014, vol. 57, # 11, p. 4834 - 4848
[2] Patent: US2009/137595, 2009, A1
[3] Patent: WO2012/116237, 2012, A2. Location in patent: Page/Page column 119
[4] Patent: US2015/320727, 2015, A1. Location in patent: Paragraph 0555; 0556
[5] Bioorganic and Medicinal Chemistry, 2015, vol. 23, # 24, p. 7585 - 7596
2-(4-AMINOPHENYL)-2-METHYLPROPANENITRILE Preparation Products And Raw materials
Raw materials2-methyl-2-(4-nitrophenyl)propanenitrile-->Stannous chloride-->Ethyl acetate
Preparation Products2-[4-[(6-Bromo-3-nitroquinolin-4-yl)amino]phenyl]-2-methylpropionitrile
Tag:2-(4-AMINOPHENYL)-2-METHYLPROPANENITRILE(115279-57-7) Related Product Information
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