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Ethyleneglycol monomethyl ether

Figure 10. Enhancement of all l aryl ether cleavage resulting from introduction of carbonyl group into para position of aromatic ring. Unimolecular rate coefficients for 4.8 X 10 M reactants in aqueous 30% ethyleneglycol monomethyl ether containing 0.53 - 0.54 M hydroxide and 0.08 - 0.09 M bisulfide at 170 C (63). Figure 10. Enhancement of all l aryl ether cleavage resulting from introduction of carbonyl group into para position of aromatic ring. Unimolecular rate coefficients for 4.8 X 10 M reactants in aqueous 30% ethyleneglycol monomethyl ether containing 0.53 - 0.54 M hydroxide and 0.08 - 0.09 M bisulfide at 170 C (63).
Tris[2-(2-methoxyethoxy)ethyl]amine (1, TDA-1). Supplier Aldrich. The reagent is obtained by reaction of the monomethyl ether of bis(ethyleneglycol), CH30-(CH2)20(CH2)20H, with ammonia at 150° catalyzed by Raney nickel. [Pg.336]

Ethyleneglycol Methylether Acetate or Glycol Monomethyl ether Acetate,... [Pg.130]

See other pages where Ethyleneglycol monomethyl ether is mentioned: [Pg.88]    [Pg.377]    [Pg.32]    [Pg.1306]    [Pg.57]    [Pg.58]    [Pg.1306]    [Pg.32]    [Pg.32]    [Pg.53]    [Pg.34]    [Pg.261]    [Pg.2241]    [Pg.2404]    [Pg.411]    [Pg.543]    [Pg.243]    [Pg.2381]    [Pg.2182]    [Pg.88]    [Pg.377]    [Pg.32]    [Pg.1306]    [Pg.57]    [Pg.58]    [Pg.1306]    [Pg.32]    [Pg.32]    [Pg.53]    [Pg.34]    [Pg.261]    [Pg.2241]    [Pg.2404]    [Pg.411]    [Pg.543]    [Pg.243]    [Pg.2381]    [Pg.2182]    [Pg.92]    [Pg.152]    [Pg.130]    [Pg.152]    [Pg.152]    [Pg.192]   
See also in sourсe #XX -- [ Pg.32 , Pg.43 ]



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Ether ethyleneglycol

Ethyleneglycol

Monomethyl

Monomethyl ether

Monomethylations

Monomethyls

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