Identification | Back Directory | [Name]
4-(PYRIDIN-3-YLOXY)-PHENYLAMINE | [CAS]
80650-45-9 | [Synonyms]
Albb-005633 IFLAB-BB F2108-0080 TIMTEC-BB SBB010739 4-(Pyridin-3-yloxy) 4-(3-pyridyloxy)aniline ASINEX-REAG BAS 10148925 4-(pyridin-3-yloxy)aniline 4-(3-Pyridinyloxy)phenylamine [4-(3-pyridyloxy)phenyl]amine 4-(PYRIDIN-3-YLOXY)-PHENYLAMINE Benzenamine,4-(3-pyridinyloxy)- 4-(pyridin-3-yloxy)aniline(SALTDATA: FREE) | [Molecular Formula]
C11H10N2O | [MDL Number]
MFCD07186369 | [MOL File]
80650-45-9.mol | [Molecular Weight]
186.21 |
Chemical Properties | Back Directory | [Melting point ]
98-105 °C(Solv: ethanol (64-17-5); water (7732-18-5)) | [Boiling point ]
346.2±22.0 °C(Predicted) | [density ]
1?+-.0.06 g/cm3(Predicted) | [storage temp. ]
Keep in dark place,Inert atmosphere,Room temperature | [form ]
solid | [pka]
4.57±0.10(Predicted) | [Appearance]
Off-white to yellow Solid |
Hazard Information | Back Directory | [Synthesis]
Synthesis of compound 34-2 (0476): To a solution of 34-1 (2.0 g, 9.259 mmol) in methanol (20 mL) was added 10% palladium/carbon (0.2 g) purged with nitrogen. Hydrogen was subsequently passed to displace the nitrogen. The reaction mixture was stirred overnight at room temperature. Upon completion of the reaction, the catalyst was removed by filtration and the filtrate was concentrated to dryness to afford 34-2 (1.7 g, 99% yield) as a brown solid. | [References]
[1] Patent: US9138427, 2015, B2. Location in patent: Page/Page column 309 [2] Patent: WO2014/176258, 2014, A1. Location in patent: Page/Page column 30 [3] Patent: WO2004/85399, 2004, A1. Location in patent: Page 168 [4] Patent: WO2005/4863, 2005, A1. Location in patent: Page/Page column 128 [5] Patent: WO2004/19941, 2004, A1. Location in patent: Page/Page column 154 |
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SynAsst Chemical.
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