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422665 Aldrich

4,5-Dichlorophthalimide

97%

  • CAS Number 15997-89-4

  • Empirical Formula (Hill Notation) C8H3Cl2NO2

  • Molecular Weight 216.02

  •  MDL number MFCD00015886

  •  PubChem Substance ID 24866447

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Properties

Related Categories Building Blocks, Carbonyl Compounds, Chemical Synthesis, Cyclic Imides, Organic Building Blocks More...
InChI Key   QJPBDGMPYPSJSF-UHFFFAOYSA-N
assay   97%
mp   217-219 °C(lit.)

Description

Packaging

5 g in glass bottle

Application

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.

Price and Availability

Safety & Documentation

Safety Information

Symbol 
GHS07  GHS07
Signal word 
Warning
Hazard statements 
Precautionary statements 
Personal Protective Equipment 
RIDADR 
NONH for all modes of transport
WGK Germany 
3

Documents

Certificate of Analysis

Protocols & Articles
Peer-Reviewed Papers
15

References

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