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3,3 -Dimethyladipic acid

Oxidation of carpamic acid with potassium permanganate or better, with nitric acid, produced an acid which, on the assumption that it was a,5-dimethyladipic acid, led Barger (33) to the erroneous conclusion that carpaine contained a substituted cyclohexane ring. Subsequent characterization of this oxidation product as a mixture of azelaic and suberic acids (34) demonstrated the presence of a chain of seven methylene groups in this base. Since the dehydrogenation of carpaine with selenium gave rise to... [Pg.99]

Dimethyladipic Acid (1 2-Dimethyl-6wtone-l - 4-dicarboxylic acid)... [Pg.890]

C8H14O4, meso-p,i3 -Dimethyladipic acid, 31B, 12 32B, 18 C8HieN202r Suberamide, 31B, 12... [Pg.12]

DIMETHYLADIPATE (627-93-0) Combustible liquid (flash point 225°F/107°C cc). Incompatible with strong acids, nitrates, oxidizers. [Pg.441]

Beilstein Handbook Reference) Adipic acid, dimethyl ester AI3-00668 BRN 1707443 DBE 6 Dimethyl adipate Dimethyl hexanedioate 1,8-Dimethylhexanedioate Dimethyladipate EINECS 211-020-6 Hexanedioic acid, dimethyl ester HSDB 5021 Methyl adipate NSC 11213. Used as a solvent and plasticizer. Liquid mp = 10.3° bpi3 = 115° d = 1.0600 insoluble in H2O, soluble in EtOH, Et20, CCI4, AcOH. DuPont Morflex UCB SA. [Pg.226]

See other pages where 3,3 -Dimethyladipic acid is mentioned: [Pg.13]    [Pg.339]    [Pg.229]    [Pg.658]    [Pg.295]    [Pg.165]    [Pg.890]    [Pg.891]    [Pg.891]    [Pg.193]    [Pg.193]    [Pg.217]    [Pg.862]    [Pg.35]    [Pg.36]    [Pg.250]    [Pg.250]    [Pg.527]    [Pg.527]    [Pg.25]    [Pg.187]    [Pg.187]    [Pg.204]    [Pg.251]    [Pg.13]    [Pg.86]   
See also in sourсe #XX -- [ Pg.13 ]



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