76892-66-5Relevant academic research and scientific papers
The Reaction of N-Aminophthalimide With Isothiocyanates
Hearn, Michael J.,Lucas, Laura E.
, p. 615 - 616 (2007/10/02)
N-Aminophthalimide (I) reacted in refluxing isopropyl alcohol with a number of isothiocyanates to give the related 1:1 addition products, N-(3-substituted thioureido)phthalimides III.On the other hand, heating I directly with an excess of neat arylisothiocyanates produced the N-arylphthalimides IV.As shown for IIIa, the 1:1 addition products are conveniently deblocked by the Ing-Manske procedure to yield the 4-substituted thiosemicarbazide.
N-(arylthiocarbamoyl)-2-amino-1H-isoindole-1,3-(2H)diones and use as plant growth regulators
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, (2008/06/13)
A novel class of compounds which are useful as plant growth regulators is disclosed, having the general structural formula: STR1 in which R1 is; C1 to C4 alkyl, nitro or halo and n is zero or an integer from 1 to 4 R2 and R3 are; H or C1 to C4 alkyl or hydroxyalkyl, or benzyl and Ar is; adamantyl, C3 to C4 alkyl or alkenyl, benzyl, halobenzyl, naphthyl, phenyl or phenyl bearing thereon from one to three of the substituents: cyano, benzyloxy, methylenedioxy, nitro, bromo, chloro, trifluoromethyl and C1 to C4 alkyl, alkenyl, alkoxy, alkylthio and alkyl-substituted amino.
