N-(6-Bromohexyl)phthalimide

97%

Reagent Code: #217498
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CAS Number 24566-79-8

science Other reagents with same CAS 24566-79-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 310.19 g/mol
Formula C₁₄H₁₆BrNO₂
badge Registry Numbers
MDL Number MFCD00023098
thermostat Physical Properties
Melting Point 58°C
Boiling Point 188 °C/0.1kPa
inventory_2 Storage & Handling
Storage Room temperature, dry

description Product Description

Used as an intermediate in organic synthesis, particularly in the preparation of functionalized polymers and dendrimers. Its bromoalkyl chain allows for further alkylation or coupling reactions, making it valuable in the development of specialty materials and pharmaceuticals. Commonly employed in the synthesis of labeled compounds, including fluorescent or radioactive probes, due to the reactivity of the bromine atom and the stability of the phthalimide group. Also utilized in the construction of ligands for catalysis and in surface modification of nanoparticles.

Available Sizes & Pricing

Size Availability Unit Price Quantity
5g
10-20 days ฿580.00
100g
10-20 days ฿10,500.00
25g
10-20 days ฿2,670.00
N-(6-Bromohexyl)phthalimide
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Used as an intermediate in organic synthesis, particularly in the preparation of functionalized polymers and dendrimers. Its bromoalkyl chain allows for further alkylation or coupling reactions, making it valuable in the development of specialty materials and pharmaceuticals. Commonly employed in the synthesis of labeled compounds, including fluorescent or radioactive probes, due to the reactivity of the bromine atom and the stability of the phthalimide group. Also utilized in the construction of ligands

Used as an intermediate in organic synthesis, particularly in the preparation of functionalized polymers and dendrimers. Its bromoalkyl chain allows for further alkylation or coupling reactions, making it valuable in the development of specialty materials and pharmaceuticals. Commonly employed in the synthesis of labeled compounds, including fluorescent or radioactive probes, due to the reactivity of the bromine atom and the stability of the phthalimide group. Also utilized in the construction of ligands for catalysis and in surface modification of nanoparticles.

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