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ChemicalBook >> CAS DataBase List >> 4,5-DICHLOROPHTHALIMIDE

4,5-DICHLOROPHTHALIMIDE

4,5-DICHLOROPHTHALIMIDE price.
  • $71.3 - $844.68
  • 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-
7 prices
Selected condition:
Brand
  • AK Scientific
  • Alichem
  • American Custom Chemicals Corporation
  • Crysdot
  • Sigma-Aldrich
  • TRC
Package
  • 100mg
  • 1g
  • 5g
  • 10g
  • ManufacturerAK Scientific
  • Product number8057AA
  • Product description5,6-Dichloroisoindoline-1,3-dione
  • Packaging1g
  • Price$179
  • Updated2021-12-16
  • Buy
  • ManufacturerAlichem
  • Product number15997894
  • Product description5,6-Dichloroisoindoline-1,3-dione
  • Packaging5g
  • Price$342.1
  • Updated2021-12-16
  • Buy
  • ManufacturerAlichem
  • Product number15997894
  • Product description5,6-Dichloroisoindoline-1,3-dione
  • Packaging10g
  • Price$520.46
  • Updated2021-12-16
  • Buy
  • ManufacturerAmerican Custom Chemicals Corporation
  • Product numberHCH0012785
  • Product description4,5-DICHLOROPHTHALIMIDE 95.00%
  • Packaging5G
  • Price$844.68
  • Updated2021-12-16
  • Buy
  • ManufacturerCrysdot
  • Product numberCD11245109
  • Product description5,6-Dichloroisoindoline-1,3-dione 95+%
  • Packaging10g
  • Price$486
  • Updated2021-12-16
  • Buy
  • ManufacturerSigma-Aldrich
  • Product number422665
  • Product description4,5-Dichlorophthalimide 97%
  • Packaging5g
  • Price$71.3
  • Updated2023-06-20
  • Buy
  • ManufacturerTRC
  • Product numberB419433
  • Product description4,5-Dichlorophthalimide
  • Packaging100mg
  • Price$75
  • Updated2021-12-16
  • Buy
Manufacturer Product number Product description Packaging Price Updated Buy
AK Scientific 8057AA 5,6-Dichloroisoindoline-1,3-dione 1g $179 2021-12-16 Buy
Alichem 15997894 5,6-Dichloroisoindoline-1,3-dione 5g $342.1 2021-12-16 Buy
Alichem 15997894 5,6-Dichloroisoindoline-1,3-dione 10g $520.46 2021-12-16 Buy
American Custom Chemicals Corporation HCH0012785 4,5-DICHLOROPHTHALIMIDE 95.00% 5G $844.68 2021-12-16 Buy
Crysdot CD11245109 5,6-Dichloroisoindoline-1,3-dione 95+% 10g $486 2021-12-16 Buy
Sigma-Aldrich 422665 4,5-Dichlorophthalimide 97% 5g $71.3 2023-06-20 Buy
TRC B419433 4,5-Dichlorophthalimide 100mg $75 2021-12-16 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): GHS hazard pictograms
Signal word: Warning
Hazard statements:
Code Hazard statements Hazard class Category Signal word Pictogram P-Codes
H315 Causes skin irritation Skin corrosion/irritation Category 2 Warning GHS hazard pictograms P264, P280, P302+P352, P321,P332+P313, P362
H319 Causes serious eye irritation Serious eye damage/eye irritation Category 2A Warning GHS hazard pictograms P264, P280, P305+P351+P338,P337+P313P
H335 May cause respiratory irritation Specific target organ toxicity, single exposure;Respiratory tract irritation Category 3 Warning GHS hazard pictograms
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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