1921
DOI: 10.1039/ct9211900664
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LXXI.—On some carbamido-acids and their hydantoins

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Cited by 6 publications
(3 citation statements)
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“…Unsymmetrical disazo 36 and trisazo 37 was applied as acid and direct dyes on wool and cotton fabrics. They had fairly good washing fastness but unsatisfactory tinctorial strength and light fastness below average was monitored [36] The fusion of 3(and 4)-nitrophthalic anhydride with aniline gave 3(and 4)-nitro-1-Nphenylphthalimide [37,38] which was exposed to reduction using tin(II) chloride and hydrochloric acid to afford the corresponding amino derivatives 38 [39] and 39 [40]. Compound 40 was condensed with 38 and 39 respectively, by refluxing for 8 hours in dry xylene and in addition to a drop of piperidine, to give 41 and 42.…”
Section: N O Omentioning
confidence: 99%
“…Unsymmetrical disazo 36 and trisazo 37 was applied as acid and direct dyes on wool and cotton fabrics. They had fairly good washing fastness but unsatisfactory tinctorial strength and light fastness below average was monitored [36] The fusion of 3(and 4)-nitrophthalic anhydride with aniline gave 3(and 4)-nitro-1-Nphenylphthalimide [37,38] which was exposed to reduction using tin(II) chloride and hydrochloric acid to afford the corresponding amino derivatives 38 [39] and 39 [40]. Compound 40 was condensed with 38 and 39 respectively, by refluxing for 8 hours in dry xylene and in addition to a drop of piperidine, to give 41 and 42.…”
Section: N O Omentioning
confidence: 99%
“…was attained momentarily. The 3-aminophthalimide (11) was prepared by the addition of 20.5 grams of the nitroamide in small portions to a solution of 90 grams of SnCl2 in 600 ml. of 10 A7 HC1.…”
Section: Methodsmentioning
confidence: 99%
“…(10) Faye, G. H., Inman, W. R., Talanta 3,277(1960). (11) Tertipis, G. G., Beamish, F. E., Anal. Chem.…”
Section: Literature Citedunclassified