| Identification | Back Directory | [Name]
4,5-DICHLOROPHTHALIMIDE | [CAS]
15997-89-4 | [Synonyms]
TIMTEC-BB SBB003388
LABOTEST-BB LT00452401
4,5-DICHLOROPHTHALIMIDE
4,5-DichlorophthaliMide 97%
5,6-dichloroisoindole-1,3-dione
1H-Isoindole-1,3(2H)-dione, 5,6-dichloro- | [Molecular Formula]
C8H3Cl2NO2 | [MDL Number]
MFCD00015886 | [MOL File]
15997-89-4.mol | [Molecular Weight]
216.02 |
| Hazard Information | Back Directory | [Uses]
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 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.
| [General Description]
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. |
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