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Acetaldehyde oximes

Individually indexed compounds are f Acetaldehyde oxime, 0865 Acetone oxime, 1258 Azoformaldoxime, 0815 Benzaldehyde oxime, 2760 Bromoacetone oxime, 1201 Butane-2,3-dione dioxime, 1595... [Pg.313]

There are three environments that we may consider for this reaction iyw-acetaldehyde oxime data in the condensed phase , the gas phase and in aqueous solution . The reaction exothermicities are 51.0, 56.5 and ca 53 kJmoD, respectively. The only other case where the values are known for all three phases is that of acetone, equation 28 ... [Pg.68]

C8H7NO3 2-Oxo-4 -hydroxyphenyl- acetaldehyde oxime Complexing agent Extraction-photometric Co, Ni, Pd Pd 81, 82... [Pg.535]

Hydroxylatnine reacts with carbonyl group =CO of aldehydes, ketones or quinones. yielding oximes, white solids, of definite melting point and used in identification of aldehydes and ketones, e.g.. acetaldehyde oxime CHtCH NOH ... [Pg.809]

AA89 C2H5NO acetaldehyde oxime QNU2 CH3CH NOH h2o PY KCI - 7 rm DME/SCE 03AO t=6.3... [Pg.28]

Acetaldehyde oxime, AA89 Acetaldehyde semicarbazone, AC08 Acetamide, AA90... [Pg.617]

Hydroquinone—oxygen clathrate, see 1,4-Benzenediol—oxygen complex, 2327 Hydroximinocyclohexane, see Cyclohexanone oxime, 2446 t Hydroximinoethane, see Acetaldehyde oxime, 0861... [Pg.2099]

Since the Pfitzinger reaction requires a large excess of alkali, aliphatic aldehydes, which readily polymerize under these conditions, cannot be used in the reaction. However, it was possible to overcome these difficulties by using the aldoximes. Thus, Pfitzinger heated the isatin 7 with acetaldehyde oxime in the presence of potassium hydroxide in water and obtained 4-quinolinecarboxylic acid together with the oxime of isatinic acid 196 [175],... [Pg.30]

Thus, acetaldehyde oxime is H3CCH=NOH and acetamide oxime is H3CC(=NOH)NH2. oxonium H30. ... [Pg.139]

Halkier, B.A., Olsen, C.E. and Muller, B.L. (1989) The biosynthesis of cyanogenic glucosides in higher plants The (E)- and (Z)-isomers of p-hydrox) heny 1-acetaldehyde oxime as intermediates in the biosynthesis of dhurrin in Sorghum bicolor (L.). Moench. /. Biol. Chem., 264,19487-94. [Pg.164]

The oximes of unsaturated carbonyl compounds react with alkenes in the presence of electrophiles to give nitrones. By contrast, the acetaldehyde oxime and iodine added to cyclohexene to give 8 in low yield as a single diastereomer, although no synthetic application of the reaction has been reported174... [Pg.796]

See other pages where Acetaldehyde oximes is mentioned: [Pg.748]    [Pg.464]    [Pg.195]    [Pg.195]    [Pg.5]    [Pg.319]    [Pg.748]    [Pg.178]    [Pg.1938]    [Pg.733]    [Pg.222]    [Pg.1301]    [Pg.396]    [Pg.126]    [Pg.5]    [Pg.755]    [Pg.1067]    [Pg.673]    [Pg.364]    [Pg.2026]    [Pg.450]    [Pg.491]    [Pg.1938]    [Pg.195]    [Pg.195]    [Pg.222]    [Pg.103]    [Pg.2]    [Pg.1488]    [Pg.83]    [Pg.322]    [Pg.1938]   
See also in sourсe #XX -- [ Pg.5 ]

See also in sourсe #XX -- [ Pg.5 ]



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C2H5NO (lZ)-Acetaldehyde oxime

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