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| | 4,5-DICHLOROPHTHALIMIDE Basic information |
| | 4,5-DICHLOROPHTHALIMIDE Chemical Properties |
| Melting point | 217-219 °C(lit.) | | density | 1.643±0.06 g/cm3(Predicted) | | storage temp. | 2-8°C | | pka | 7.84±0.20(Predicted) |
| Hazard Codes | Xi | | Risk Statements | 36/37/38 | | Safety Statements | 26-36 | | WGK Germany | 3 |
| | 4,5-DICHLOROPHTHALIMIDE Usage And Synthesis |
| 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. |
| | 4,5-DICHLOROPHTHALIMIDE Preparation Products And Raw materials |
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