5-Bromo-isoindole-1,3-dione

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Reagent Code: #144390
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Alias 5-Bromoisoindole-1,3-dione; 4-Bromophthalimide
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CAS Number 6941-75-9

science Other reagents with same CAS 6941-75-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 226.03 g/mol
Formula C₈H₄BrNO₂
badge Registry Numbers
MDL Number MFCD00466049
inventory_2 Storage & Handling
Storage Room temperature, sealed

description Product Description

Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and bioactive compounds. Its bromine functionality allows for cross-coupling reactions, such as Suzuki or Heck reactions, enabling the construction of complex heterocyclic systems. Commonly employed in the development of medicinal agents where isoindole derivatives exhibit antimicrobial, anti-inflammatory, or anticancer activities. Also utilized in materials science for synthesizing functional dyes and optoelectronic materials due to its aromatic and electron-deficient structure.

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Test Parameter Specification
Purity 96.5-100
Melting point 230-235°C
Appearance White to off-white powder

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿132.00
inventory 5g
10-20 days ฿440.00
inventory 25g
10-20 days ฿2,110.00
inventory 100g
10-20 days ฿8,350.00

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5-Bromo-isoindole-1,3-dione
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Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and bioactive compounds. Its bromine functionality allows for cross-coupling reactions, such as Suzuki or Heck reactions, enabling the construction of complex heterocyclic systems. Commonly employed in the development of medicinal agents where isoindole derivatives exhibit antimicrobial, anti-inflammatory, or anticancer activities. Also utilized in materials science for synthesizing functional dyes and optoel

Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and bioactive compounds. Its bromine functionality allows for cross-coupling reactions, such as Suzuki or Heck reactions, enabling the construction of complex heterocyclic systems. Commonly employed in the development of medicinal agents where isoindole derivatives exhibit antimicrobial, anti-inflammatory, or anticancer activities. Also utilized in materials science for synthesizing functional dyes and optoelectronic materials due to its aromatic and electron-deficient structure.

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