4,5-DICHLOROPHTHALIMIDE

₹5260
Product name: 4,5-DICHLOROPHTHALIMIDE
CAS: 15997-89-4
MF: C8H3Cl2NO2
MW: 216.02
EINECS:
MDL Number:MFCD00015886
Synonyms:4,5-DichlorophthaliMide 97%;TIMTEC-BB SBB003388;4,5-DICHLOROPHTHALIMIDE;LABOTEST-BB LT00452401;5,6-dichloroisoindole-1,3-dione;1H-Isoindole-1,3(2H)-dione, 5,6-dichloro-;4,4'-Oxydibenzenesulfonohydrazide

Price1 Properties Safety Information Description

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Brand

Sigma-Aldrich(India)

Package

ManufacturerSigma-Aldrich(India)
Product number422665
Product description4,5-Dichlorophthalimide 97%
Packaging5G
Price₹5260
Updated2022-06-14
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Manufacturer	Product number	Product description	Packaging	Price	Updated	Buy
Sigma-Aldrich(India)	422665	4,5-Dichlorophthalimide 97%	5G	₹5260	2022-06-14	Buy

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)

Safety Information

Symbol(GHS):

Signal word:

Warning

Hazard statements:

Code	Hazard statements	Hazard class	Category	Signal word	P-Codes
H315	Causes skin irritation	Skin corrosion/irritation	Category 2	Warning	P264, P280, P302+P352, P321,P332+P313, P362
H319	Causes serious eye irritation	Serious eye damage/eye irritation	Category 2A	Warning	P264, P280, P305+P351+P338,P337+P313P
H335	May cause respiratory irritation	Specific target organ toxicity, single exposure;Respiratory tract irritation	Category 3	Warning

Precautionary statements:

P261	Avoid breathing dust/fume/gas/mist/vapours/spray.
P264	Wash hands thoroughly after handling.
P264	Wash skin thouroughly after handling.
P271	Use only outdoors or in a well-ventilated area.
P280	Wear protective gloves/protective clothing/eye protection/face protection.
P302+P352	IF ON SKIN: wash with plenty of soap and water.
P305+P351+P338	IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.

Description

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’-dideoxythymidineand 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 ofN-(3-bromopropyl)-4,5-dichlorophthalimide.As a nucleophilic partner in the phosphine-catalyzed allylic substitution of Morita-Baylis-Hillman acetates to formN-protected β-amino phosphonic acid esters.

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