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Oxoacetic acid

CH4N2 463-52-5) see Itraconazole formamidine hydrochloride (CH5QN2 6313-33-3) sec Allopurinol 7-formamidocephalosporanic acid (CiiHj2N20fiS 27267-35-2) see Cefamandole 2-(2-formamido-4-thiazolyl)-2-methoxyiminoacetic acid (C7H7N3O4S 83594-38-1) see Ceftizoxime (2-formamidothiazol-4-yl)oxoacetic acid (CfiH4N204S 64987-06-0) see Cetixime formic acid... [Pg.2389]

The following analytical standards were synthesized by Monsanto Company and may be available through the Environmental Protection Agency, National Pesticide Standard Repository (Fort Meade, MD, USA) [l-(methylethyl)phenylamino] oxoacetic acid, sodium salt, >95% pure (NIPA-producing metabolite) and N-isopropylaniline (NIPA), >99% pure. [Pg.363]

The established procedure for the synthesis of the fused pyrazine ring involves condensation of the oxadiazole diamine with 1,2-dicarbonyl compounds <1978JOC341>. The latter procedure was used by Beebe et al. to make a series of [l,2,5]oxadiazolo[3,4-/ ]pyrazines for evaluation as antibacterial agents <2003BML3133>. An example is shown in Scheme 52, which involved heating the diamine with (3-bromophenyl)oxoacetic acid in glacial acetic acid at 110°C to give the [l,2,5]oxadiazolo[3,4- ]pyrazine. [Pg.684]

Oxiranemethanol nitrate, see 2,3-Epoxypropyl nitrate, 1182 Oxiranemethanol, see 2,3-Epoxypropanol, 1225 Oxoacetic acid, see Glyoxylic acid, 0720 Oxobis[aqua(oxo)diperoxorheniumVII], 4532 /(-Oxo-/,/-bis(trifhioroacetato-<9)-/,/-diphenyldiodine(III), 3691 Oxodiperoxodipiperidinechromium(VI), 3361 Oxodiperoxodipyridinechromium(VI), 3268 Oxodiperoxodi(pyridine /V-ox ide)mol ybdenu m, 3273 Oxodiperoxodi(pyridine /V-oxide)tungsten, 3277 Oxodiperoxodiquinolinechromium( VI), 3742 Oxodiperoxomolybdenum—hexamethylphosphoramide, 4713 Oxodiperoxopyridinechromium V-oxide, 1838... [Pg.2120]

Glyoxylic acid (= Oxoacetic acid) (carboxylic acid) Universal unripe fruit, young leaf Beta vulgaris (young sugar beet) (Chenopodiaceae), Ribes uva-crispa (Grossulariaceae) [fruit] Sour (acid) taste [irritant]... [Pg.416]

Dicarbonyl compounds can be cleaved oxidatively using peracids this protocol has been used to prepare cyclopropanecarboxylic acids from a dicyclopropylethanedione, e.g. 2 from 1 and several 2-cyclopropyl-2-oxoacetic acids. " An appropriately substituted 1,3-diketone has also been converted to a cyclopropanecarboxylic acid by basic hydrolysis. When a hydroxy group is attached p to the carbonyl group of an alkyl cyclopropyl ketone, periodate oxidation afforded a similar acid in quantitative yield. ... [Pg.1750]

In a similar way, hydrazones of (2-carboxy-3-pyridyl)oxoacetic acid are cyclized either thermally or by acid catalysis to 4b,c.38... [Pg.14]

Furthermore reaction of 62 with 331 and ultraviolet light gave the same products 332 and 333 but in 17 and 40% yield, respectively (Scheme 104). On the other hand, reaction of 62 and 334 gave also the same product 335, in 14% yield together with [indol-3-ylideneamino)-5-fluorophenyl]oxoacetic acid 338 in 37% yield. [Pg.196]

The presence of acetic acid, oxo-, oxoacetic acid, glyoxylic acid, glyoxalic acid (298-12-4] in roasted coffee has been suggested by Van der Stegen and Van Duijn (1988). [Pg.160]

CAS 298-12-4 EINECS/ELINCS 206-058-5 Synonyms Acetic acid, oxo- Formylformic acid Glyoxalate Glyoxylate a-Ketoacetic acid Oxaldehydic acid Oxoacetic acid Oxoethanoic acid... [Pg.1943]

Oxirane, phenyl-. See Styrene oxide Oxirane, (trichloromethyl)-. See 1,2-Epoxy-3,3,3-trichloropropane Oxirane, trifluoro (trifluoromethyl)-. See 1,2-Epoxy-1,1,2,3,3,3-hexafluoropropane Oxirene, 2,2,2-trichloroethyl-. See Trichlorobutylene oxide Oxitol. See Ethoxyethanol Oxoacetic acid. See Glyoxalic acid 5-Oxobarbituric acid monohydrate. See Alloxan monohydrate... [Pg.3010]

Oxoacetic acid, 9CI. Glyoxalic acid. Aldehydoformic acid. Formylformic acid. Oxalaldehydic acid [298-12-4]... [Pg.588]

The aldehyde component has also been replaced by diethyl formylphosphonate hydrate in the silver-catalyzed synthesis of V-PMP-protected a-aminopropargylphospho-nates [139] and by 2-oxoacetic acid [140] or glyoxylic acid [141] in copper-catalyzed microwave-assisted decarboxyla-tive three-component couplings. In addition, glyoxylic acid has been coupled with amines and alkynes in the gold-catalyzed synthesis of butenolides (see Scheme 3.48) [121]. [Pg.99]

H. Feng, D. S. Ermolat ev, G. Song, E. V. Van der Eycken, J. Org. Chem. 2011, 76, 7608—7613. Microwave-assisted decarboxylative three-component couphng of a 2-oxoacetic acid, an amine, and an alkyne. [Pg.123]


See other pages where Oxoacetic acid is mentioned: [Pg.890]    [Pg.806]    [Pg.276]    [Pg.1159]    [Pg.722]    [Pg.834]    [Pg.308]    [Pg.269]    [Pg.269]    [Pg.2038]    [Pg.124]    [Pg.196]    [Pg.522]    [Pg.709]    [Pg.311]    [Pg.1043]    [Pg.455]    [Pg.95]    [Pg.298]    [Pg.571]    [Pg.204]    [Pg.204]    [Pg.543]    [Pg.1096]    [Pg.65]    [Pg.66]   
See also in sourсe #XX -- [ Pg.3 , Pg.10 ]

See also in sourсe #XX -- [ Pg.2 , Pg.95 ]

See also in sourсe #XX -- [ Pg.298 ]

See also in sourсe #XX -- [ Pg.204 ]

See also in sourсe #XX -- [ Pg.65 ]




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