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1.3- Propanedicarboxylic acid

Propanedicarboxylic acid, gl4 Propanedioic acid, m3 1,2-Propanediol cyclic carbonate, p230 Propanenitrile, p215... [Pg.303]

Methy1propanaI N,N-dimethyl-N-ethyl-2-ammonium iodide, A033 2-Methyl-1,3-propanedicarboxylic acid, AH80... [Pg.637]

Synthesis of substituted acetic acid via malonic ester Malonic ester is an ester formed by reacting an alcohol with malonic acid (propanedicarboxylic acid). Following is the structure of diethyl malonate ... [Pg.150]

Schwarz A, Oberhausen E, Schroth HJ, Hale TJ (1991) Teceos. Scientific information on the labeling unit technetium-99m-3,3-diphosphono-l,2-propanedicarboxylic acid. Behring Diagnostika, Marburg, Germany... [Pg.290]

Beilstein Handbook Reference) AI3-24247 BRN 1209725 EINECS 203-817-2 Glutaric acid HSDB 5542 NSC 9238 Pentandioic acid Pentanedioic acid 1,5-Pentanedioic acid 1,3-Propanedicarboxylic acid n-Pyrotartaric acid. Needles mp = 97.8 bp = 303° (dec) d = 1,429 very soluble in H2O, EtOH, EtpO soluble in CHCI3, cone, H2SO4 slightly soluble in DMSO, ligroin insoluble In CsHe. [Pg.305]

CAS 110-94-1 El NECS/ELINCS 203-817-2 Synonyms Pentandioic acid Pentanedioic acid 1,5-Pentanedioic acid Pentane-1,5-dioic acid 1,3-Propanedicarboxylic acid... [Pg.1895]

The incorporation of cyclic carbohydrates into Gemini surfactants was developed by Castro et al. (Rg. 7.27) [56]. These sugar geminis have been synthesized from AGs which can be easily prepared via a Rsher-type glycosylation reaction of free glucose by w-butanol. Convenient protection of the sugar moiety, followed by selective deprotection of the primary alcohol, permits the formation of gemini 12 by a double esterification with propanedicarboxylic acid. [Pg.171]

Two specific j8-dicarbonyl compounds have had broad use in organic synthesis. These are acetoacetic ester (ethyl acetoacetate, ethyl 3-oxobutanoate), which can be used to make substituted acetone derivatives, and diethyl malonate (diethyl 1,3-propanedicarboxylic acid), which can be used to make substituted acetic acid derivatives. We shall consider syntheses involving ethyl acetoacetate and diethyl malonate in the upcoming sections of this chapter. [Pg.835]

See other pages where 1.3- Propanedicarboxylic acid is mentioned: [Pg.362]    [Pg.415]    [Pg.402]    [Pg.162]    [Pg.52]    [Pg.3713]    [Pg.835]    [Pg.27]    [Pg.830]    [Pg.351]    [Pg.201]    [Pg.201]    [Pg.201]    [Pg.201]    [Pg.201]    [Pg.868]   
See also in sourсe #XX -- [ Pg.3 , Pg.10 ]



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