Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Ethyl-4,4-dimethyl-1,3-oxazolidine

Oxa-3-azaindene. See Benzoxazole Oxaban -A. See Dimethyl oxazolidine Oxaban -E. See 7-Ethyl bicyclooxazolidine 7-Oxabicyclo [4.1.0] heptane. See Cyclohexene... [Pg.3004]

Oxazolidine A. See Dimethyl oxazolidine Oxazolidine-5-carboxylic acid, 3-(3,5-dichlorophenyl)-2,4-dioxo-5-methyl-, ethyl ester. See Chlozolinate Oxazolidinone CAS 70-07-5... [Pg.3008]

Dicocodimonium chloride Glutaral biocide, oil field chemicals Dimethyl oxazolidine biocide, oil field water systems 7-Ethyl bicyclooxazolidine biocide, oil recovery Tributyltin oxide biocide, oil well brines Methylenebis (thiocyanate) biocide, paints... [Pg.4907]

Dodecylguanidine hydrochloride biocide, recirculating water systems Dimethyl oxazolidine biocide, resin emulsions 7-Ethyl bicyclooxazolidine 2[(-Hydroxymethyl) amino] ethanol biocide, rubber... [Pg.4908]

Calcium undecylenate L-Camphor Cetalkonium chloride Cetearalkonium bromide Cetrimonium bromide Cetrimonium chloride Cetylpyridinium chloride Chlorhexidine Chlorhexidine diacetate Chlorhexidine digluconate Chlorhexidine dihydrochloride Chloroacetamide Chlorobutanol Chlorophene Chloroxylenol Chlorphenesin Climbazole o-Cymen-5-ol Diazolidinyl urea Dilauryl thiodipropionate Dimethyl hydantoin-formaldehyde polymer Dimethylhydroxymethylpyrazole Dimethyl oxazolidine DM DM hydantoin Edetic acid Ethyl benzoate Ethylparaben Ethyl vanillate Fluorosalan Formaldehyde Formic acid Glutaral Grapefruit (Citrus grandis) seed extract Hexamethylenetetramine Hexamidine... [Pg.5563]

Cyclization of dimethyl ( S)-malate (2) with methyl or ethyl isocyanate affords oxazolidin-2,4-diones (174) in 60 or 62% yield, respectively. This heterocyclic system provides the basic... [Pg.190]

Asym. synthesis. D(-)-Ephedrine hydrate and p-chlorobenzaldehyde refluxed 1 hr. in benzene, then the calculated amount of water removed using a Dean-Stark column (2R 4S 5R)-2-chlorophenyl-3,4-dimethyl-5-phenyloxazolidine. Y ca. 100%. - The induced asym. center in position 2 has the R conflguration. On degradation, the oxazolidines yield optically pure a-arylethylamines or a-aryl-ethyl halides. F. e. s. L. Neelakantan, J. Org. Chem. 36, 2256, 2253 (1971) carbohydrate derivs. s. H. Dorn and D. Arndt, Z. Chem. 77, 306 (1971). [Pg.439]

See other pages where Ethyl-4,4-dimethyl-1,3-oxazolidine is mentioned: [Pg.381]    [Pg.5566]    [Pg.5566]    [Pg.2114]    [Pg.1072]    [Pg.79]    [Pg.80]    [Pg.90]    [Pg.56]    [Pg.61]    [Pg.226]    [Pg.555]    [Pg.767]    [Pg.496]    [Pg.41]    [Pg.46]    [Pg.212]    [Pg.11]    [Pg.122]    [Pg.20]   
See also in sourсe #XX -- [ Pg.3 , Pg.122 ]



SEARCH



1,2-Oxazolidin

5.6- Dimethyl-2-[2- -ethyl

Oxazolidine

Oxazolidines

© 2024 chempedia.info