Identification | More | [Name]
Phenyl 2-pyridyl ketoxime | [CAS]
1826-28-4 | [Synonyms]
2-BENZOYLPYRIDINE KETOXIME PHENYL 2-PYRIDYL KETONE OXIME PHENYL 2-PYRIDYL KETOXIME PHENYL-ALPHA-PYRIDYL KETOXIME PHENYL-A-PYRIDYL KETOXIME PPKO SYN-PHENYL-2-PYRIDYLKETOXIME TIMTEC-BB SBB008988 (Z)-Phenyl(2-pyridinyl)methanone oxime Ketone, phenyl 2-pyridyl, oxime Methanone, phenyl-2-pyridinyl-, oxime phenyl-2-pyridinyl-methanonoxime Phenyl-pyridin-2-yl-methanone oxime Phenylpyridylketoxime 2-Benzoylpyridine oxime 2-Benzoylpyridiineketoxime Phenyl 2-pyridyl ketoxime, 98+% (2-Pyridyl)phenyl ketoneoxime 2-Pyridylphenyl ketoneoxime PPKO【Dotite】 | [EINECS(EC#)]
217-374-8 | [Molecular Formula]
C12H10N2O | [MDL Number]
MFCD00006310 | [Molecular Weight]
198.22 | [MOL File]
1826-28-4.mol |
Safety Data | Back Directory | [Hazard Codes ]
T,Xi | [Risk Statements ]
R25:Toxic if swallowed. R37/38:Irritating to respiratory system and skin . R41:Risk of serious damage to eyes. R36/37/38:Irritating to eyes, respiratory system and skin . | [Safety Statements ]
S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice . S36/37/39:Wear suitable protective clothing, gloves and eye/face protection . S45:In case of accident or if you feel unwell, seek medical advice immediately (show label where possible) . S37/39:Wear suitable gloves and eye/face protection . | [RIDADR ]
UN 2811 6.1/PG 3
| [WGK Germany ]
3
| [TSCA ]
Yes | [HazardClass ]
6.1 | [HS Code ]
29333990 |
Hazard Information | Back Directory | [Chemical Properties]
Slightly pinl crystalline powder | [Uses]
Phenyl 2-pyridyl ketoxime was used in preparation of inverse-9-metallacrown-3, trinuclear clusters. | [General Description]
The complexation reaction of phenyl 2-pyridyl ketoxime with some transition and heavy metal ions Co2+, Ni2+, Zn2+, Pb2+, Fe2+, Fe3+, Cr3+ and La2+ has been studied potentiometrically. The reactions of phenyl(2-pyridyl)ketone oxime, with nickel(II) sulfate hexahydrate, in the absence of an external base, have been investigated. | [Purification Methods]
The E-isomer crystallises from EtOH (charcoal). It isomerizes to the Z-isomer on melting or in boiling o-xylene, and crystallises from EtOH or cyclohexanol with m 166-168o. [Beilstein 21 H 330, 21 III/IV 4120, 21/8 V 568.] |
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Alfa Aesar
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Energy Chemical
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TCI Europe
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