| Identification | More | [Name]
5-AMINO-3-PHENYLISOXAZOLE | [CAS]
4369-55-5 | [Synonyms]
3-PHENYL-5-ISOXAZOLAMINE
3-PHENYLISOXAZOL-5-AMINE
3-PHENYL-ISOXAZOL-5-YLAMINE
3-PHENYLISOXAZOLE-5-AMINE
5-AMINO-3-PHENYLISOXAZOLE
AKOS B029446
OTAVA-BB BB7020410006
SALOR-INT L482897-1EA
5-Isoxazolamine,3-phenyl-(9CI)
5-Amino-3-phenylisoxazole ,97% | [Molecular Formula]
C9H8N2O | [MDL Number]
MFCD00464114 | [Molecular Weight]
160.17 | [MOL File]
4369-55-5.mol |
| Chemical Properties | Back Directory | [Melting point ]
110-114 °C(lit.) | [Boiling point ]
379.3±30.0 °C(Predicted) | [density ]
1.204±0.06 g/cm3(Predicted) | [storage temp. ]
Keep in dark place,Sealed in dry,Room Temperature | [solubility ]
soluble in Methanol | [form ]
Crystalline Powder | [pka]
-1.69±0.10(Predicted) | [color ]
Orange | [Detection Methods]
HPLC | [CAS DataBase Reference]
4369-55-5(CAS DataBase Reference) |
| Hazard Information | Back Directory | [Chemical Properties]
Yellow solid | [Synthesis]
GENERAL METHOD: Benzoylacetonitrile (100 mmol) was added to 15% aqueous sodium hydroxide solution (100 mL) followed by hydroxylamine (200 mmol). The reaction mixture was heated to reflux for 14 h. After cooling to room temperature, the resulting precipitate was separated by filtration and recrystallized with isopropanol. | [References]
[1] Bioorganic and Medicinal Chemistry, 2017, vol. 25, # 6, p. 1914 - 1925
[2] Organic Letters, 2017, vol. 19, # 4, p. 934 - 937
[3] Organic Letters, 2018, vol. 20, # 9, p. 2774 - 2777
[4] Journal of Medicinal Chemistry, 2012, vol. 55, # 3, p. 1082 - 1105
[5] Patent: EP1813606, 2007, A1. Location in patent: Page/Page column 81 |
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