ChemicalBook--->CAS DataBase List--->15997-89-4

15997-89-4

15997-89-4 Structure

15997-89-4 Structure
IdentificationBack 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
Chemical PropertiesBack Directory
[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)
[Appearance]

White to off-white Solid
[InChI]

1S/C8H3Cl2NO2/c9-5-1-3-4(2-6(5)10)8(13)11-7(3)12/h1-2H,(H,11,12,13)
[InChIKey]

QJPBDGMPYPSJSF-UHFFFAOYSA-N
[SMILES]

Clc1cc2C(=O)NC(=O)c2cc1Cl
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319-H335
[Precautionary statements ]

P261-P264-P271-P280-P302+P352-P305+P351+P338
[Hazard Codes ]

Xi
[Risk Statements ]

36/37/38
[Safety Statements ]

26-36
[WGK Germany ]

3
[Storage Class]

11 - Combustible Solids
[Hazard Classifications]

Eye Irrit. 2
Skin Irrit. 2
STOT SE 3
Hazard InformationBack 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.
Spectrum DetailBack Directory
[Spectrum Detail]

4,5-DICHLOROPHTHALIMIDE(15997-89-4)1HNMR
4,5-DICHLOROPHTHALIMIDE(15997-89-4)IR
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