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5-Iodosalicylic acid

Iodosalicylic acid (2-hydroxy-5-iodobenzoic acid) [119-30-2] M 264.0, m 197 pKj 2.65, pK 13.05. Crystd from water. [Pg.270]

Stadeler s discovery of the formation of chloranil from tyrosine led to the supposition that tyrosine was a derivative of salicylic acid, and on this assumption Schmidt and Nasse attempted to synthesise tyrosine from ethylamine and iodosalicylic acid, and from amidosalicylic and ethyl iodide, but did not succeed. On heating tyrosine they obtained a base CgHuNO, which they thought analogous to the one Schmidt had obtained by heating amidosalicylic acid on this account they held to the accuracy of the theory that tyrosine was ethylamidosalicylic acid. [Pg.41]

See under 4-Iodosalicylic Acid. 1-Iodonaphthalene [oi-Iodonaphthalene, a-naphthyl iodtde)... [Pg.384]

Spacer. After iodination to the 4-Azido-3- iodosalicylic acid derivative it was found suitable for the radioactive labelling of avermectin binding proteins. The... [Pg.70]

See other pages where 5-Iodosalicylic acid is mentioned: [Pg.246]    [Pg.238]    [Pg.246]    [Pg.246]    [Pg.276]    [Pg.228]    [Pg.270]    [Pg.302]    [Pg.246]    [Pg.238]    [Pg.246]    [Pg.246]    [Pg.38]    [Pg.276]    [Pg.20]    [Pg.228]    [Pg.270]    [Pg.240]    [Pg.240]    [Pg.302]    [Pg.80]    [Pg.876]    [Pg.395]    [Pg.395]    [Pg.80]    [Pg.402]    [Pg.336]    [Pg.313]   
See also in sourсe #XX -- [ Pg.367 ]



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5-Iodosalicylate

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