o-chlorobenzaldoxime
o-chlorobenzaldoxime structure
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Common Name | o-chlorobenzaldoxime | ||
|---|---|---|---|---|
| CAS Number | 3717-28-0 | Molecular Weight | 155.58200 | |
| Density | 1.21g/cm3 | Boiling Point | 242.6ºC at 760mmHg | |
| Molecular Formula | C7H6ClNO | Melting Point | 73-76 °C(lit.) | |
| MSDS | Chinese USA | Flash Point | 100.5ºC | |
| Symbol |
GHS07 |
Signal Word | Warning | |
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A mild and selective method for the conversion of oximes into ketones and aldehydes by the use of N-bromophthalimide. Khazaei A, et al.
J. Chem. Res. (M) 2004(10) , 695-696, (2004)
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Solid-phase synthesis of 5-isoxazol-4-yl-[1,2,4] oxadiazoles. Quan C and Kurth M.
J. Org. Chem. 69(5) , 1470-1474, (2004)
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Amberlyst 15 supported nitrosonium ion as an efficient reagent for regeneration of carbonyl compounds from oximes, hydrazones and semicarbazones. Lakouraj MM, et al.
Reactive funct. Polym. 66(9) , 910-915, (2006)
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Facile and Chemoselective Microwave-Assisted Cleavage of Oximes to Their Corresponding Carbonyl Compounds Using N,N′-Dibromo-N,N′-1,3-propylene-bis[(4-methylphenyl)sulfonamide] as a Deoximating Reagent. Khazaei A, et al.
Synthesis 2004(17) , 2784-2786, (2004)
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Microwave-assisted chemoselective cleavage of oximes to their corresponding carbonyl compounds using 1, 3-dichloro-5, 5-dimethyl-hydantoin (DCDMH) as a new Deoximating reagent. Khazaei A and Manesh AA.
Synthesis 2005(12) , 1929-1931, (2005)
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Hypervalent iodine mediated synthesis of di-and tri-substituted isoxazoles via [3+2] cycloaddition of nitrile oxides. Singhal A, et al.
Tetrahedron 57(7) , 719-722, (2016)
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Design, synthesis and antibacterial activity of novel N-formylhydroxylamine derivatives as PDF inhibitors. Yin L, et al.
Indian J. Chem. B 50(5) , 695, (2011)
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