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Dichloroethanoic acid

Dichloroethanoic acid, CHCljCOOH. Low-melting solid, m.p. 5-6 "C, b.p. 194°C. Prepared by the action of copper powder on trichloroethanoic acid or by the action of sodium cyanide on chloral hydrate. [Pg.94]

SYNS BICHLORACETIC ACID DCA DICHLORETHANOIC ACID 2,2-DICHLOROACETIC ACID DICHLOROETHANOIC ACID D KYSELINA DICHLOROCTOVA URNER S LIQUID... [Pg.452]

DICHLOROETHANE see EIY600 sym-DICHLOROETHANE see EIY600 DICHLORO-l,2-ETHANE (FRENCH) see EIY600 a,P-DICHLOROETHANE see EIY600 DICHLOROETHANOIC ACID see DELOOO DICHLOROETHANOYL CHLORIDE see DEN400... [Pg.1619]

Common Name Dichloroacetic acid Synonym dichloroethanoic acid Chemical Name dichloroacetic acid CAS Registry No 79-43-6 Molecular Formula CjHjCljOj, CljCHCOOH Molecular Weight 128.942 Melting Point (°C) ... [Pg.471]

Dichloroacetic acid (Figure 12.4), also known as bichloroacetic acid and dichloroethanoic acid, has a molecular weight of 128.94 and a pK of 1.3. It is soluble in water, alcohol and ether. [Pg.80]

DICHLOROETHANOIC ACID (79-43-6) A medium-strong acid incompatible with nonoxidiziiig mineral acids, organic acids, bases, acrylates, aldehydes, alcohols, alkylene oxides, ammonia, aliphatic amines, alkanolamines, aromatic amines, amides, glycols, isocyanates, ketones. Attacks metals, generating flammable hydrogen gas. Attacks some plastics, rubber, and coatings. [Pg.400]

Synonyms Bichloracetic acid DCA Dichloracetic acid Dichlorethanoic acid 2,2-Dichloroacetic acid Dichloroethanoic acid... [Pg.1253]

Chloroacetic acid (chloroethanoic acid), CH2CICOOH Dichloroacetic acid (dichloroethanoic acid), CHCI2COOH Trichloroacetic acid (trichloroethanoic acid), CCI3COOH... [Pg.79]

The selective a-chlorination of propanoic acid to 2-chloro- and 2,2-dichloropro-panoic acid at 80-130 °C in the presence of chlorosulfonic and dichloroethanoic acid as catalysts and oxygen as the radical scavenger was examined. The results confirmed previous studies (Chapter 5, Section 5.6), indicating that the intermediate was propanoyl chloride formed from propanoic acid and chlorosulfonic acid by acid-catalysed enolization and substitution of the hydroxyl group by chlorine. [Pg.280]

Which acid has the larger p/f, chloroethanoic acid ((CICH CO H) or dichloroethanoic acid ((Cl CHCO H) Why Based on the pA values of substituted butanoic acids (Section 3.4), predict the pA of 4-chlorobutanoic acid. [Pg.104]

See other pages where Dichloroethanoic acid is mentioned: [Pg.799]    [Pg.326]    [Pg.63]    [Pg.88]    [Pg.236]    [Pg.1263]    [Pg.848]    [Pg.41]    [Pg.669]    [Pg.404]    [Pg.2071]    [Pg.310]    [Pg.999]    [Pg.49]    [Pg.69]   
See also in sourсe #XX -- [ Pg.821 ]



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