4,5-二氯酞酰亚胺，15997-89-4，97%

中文名：4,5-二氯酞酰亚胺

英文名：4,5-Dichlorophthalimide

中文别名：5,6-二氯-1H-异吲哚-1,3(2H)-二酮

英文别名：4,5-Dichlorophthalimide|15997-89-4|5,6-dichloroisoindoline-1,3-dione|5,6-dichloroisoindole-1,3-dione|1H-Isoindole-1,3(2H)-dione, 5,6-dichloro-|5,6-dichloro-2,3-dihydro-1H-isoindole-1,3-dione|NSC72067|1H-Isoindole-1,3(2H)-dione,5,6-dichloro-|NCIOpen2_00370

纯度：97%

货号：D167653

Cas号：15997-89-4

存储温度：室温

产品介绍：

4,5-Dichlorophthalimide (5,6-dichloro-1H-isoindole-1,3(2H)-dione) is a phthalimide derivative. It has been synthesized from 5,6-dichloro-1,3-isobenzofurandione and characterized by 1H ,13C-NMR and IR.The dipole moment, polarizability and first-order hyperpolarizability of 4,5-dichlorophthalimide have been investigated using ab initio and density functional theory calculations.4,5-Dichlorophthalimide (5,6-dichloro-1H-isoindole-1,3(2H)-dione) is suitable as a reactant in the synthesis of 5’-N-(4’’,5’’-dichlorophthaloyl)-3’-azido-2’,3’-dideoxythymidine[2] and 2-amino-4,5-dichlorobenzoic acid. It may be used in the following studies: · As a reactant in the synthesis of 4,5-dichloro-1,2-benzenedicarboxamide. · As an additive in the Ir-BICP catalyzed asymmetric hydrogenation of 2,3,3-trimethylindolenine to improve enantioselectivity. · As a reactant in the synthesis of octachloro-Cu-phthalocyanine. · As a reagent in the synthesis of 7-tert-butylthianthrene-2,3-dicarboxylic imide. · As a starting material in the synthesis of N-(3-bromopropyl)-4,5-dichlorophthalimide. · As a nucleophilic partner in the phosphine-catalyzed allylic substitution of Morita-Baylis-Hillman acetates to form N-protected β-amino phosphonic acid esters.

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