2-Iodo-4-nitrobenzyl Bromide

≥95%

Reagent Code: #201210
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CAS Number 89642-21-7

science Other reagents with same CAS 89642-21-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 341.93 g/mol
Formula C₇H₅BrINO₂
badge Registry Numbers
MDL Number MFCD18398003
inventory_2 Storage & Handling
Storage 2-8°C, light-proof, inert gas

description Product Description

Used primarily as an intermediate in organic synthesis, especially in the preparation of pharmaceuticals and agrochemicals. Its dual halogen functionality allows for selective cross-coupling reactions, making it valuable in constructing complex aromatic molecules. Commonly employed in the development of dyes and fluorescent probes due to its ability to modify aromatic systems with electron-withdrawing groups. Also utilized in research settings for synthesizing benzylated compounds and in the formation of heterocyclic structures through cyclization reactions.

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inventory 1g
10-20 days ฿10,970.00

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2-Iodo-4-nitrobenzyl Bromide
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Used primarily as an intermediate in organic synthesis, especially in the preparation of pharmaceuticals and agrochemicals. Its dual halogen functionality allows for selective cross-coupling reactions, making it valuable in constructing complex aromatic molecules. Commonly employed in the development of dyes and fluorescent probes due to its ability to modify aromatic systems with electron-withdrawing groups. Also utilized in research settings for synthesizing benzylated compounds and in the formation of

Used primarily as an intermediate in organic synthesis, especially in the preparation of pharmaceuticals and agrochemicals. Its dual halogen functionality allows for selective cross-coupling reactions, making it valuable in constructing complex aromatic molecules. Commonly employed in the development of dyes and fluorescent probes due to its ability to modify aromatic systems with electron-withdrawing groups. Also utilized in research settings for synthesizing benzylated compounds and in the formation of heterocyclic structures through cyclization reactions.

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