4-Bromo-2-(chloromethyl)-1-iodobenzene

95%

Reagent Code: #119267
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CAS Number 1261817-10-0

science Other reagents with same CAS 1261817-10-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 331.38 g/mol
Formula C₇H₅BrClI
badge Registry Numbers
MDL Number MFCD18391683
inventory_2 Storage & Handling
Storage -20°C

description Product Description

This compound is primarily utilized in organic synthesis as a versatile intermediate for constructing complex aromatic structures. Its functional groups, including bromo, chloromethyl, and iodo substituents, make it highly reactive in cross-coupling reactions, such as Suzuki or Sonogashira couplings, enabling the formation of carbon-carbon bonds. It is also employed in the preparation of pharmaceuticals and agrochemicals, where its halogenated aromatic core serves as a key building block. Additionally, its reactivity allows for further functionalization, making it valuable in material science for developing advanced polymers or organic electronic materials.

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Test Parameter Specification
Appearance Off-white to Beige Powder
Purity (%) 97.5-100
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿2,142.00
inventory 1g
10-20 days ฿5,247.00

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4-Bromo-2-(chloromethyl)-1-iodobenzene
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This compound is primarily utilized in organic synthesis as a versatile intermediate for constructing complex aromatic structures. Its functional groups, including bromo, chloromethyl, and iodo substituents, make it highly reactive in cross-coupling reactions, such as Suzuki or Sonogashira couplings, enabling the formation of carbon-carbon bonds. It is also employed in the preparation of pharmaceuticals and agrochemicals, where its halogenated aromatic core serves as a key building block. Additionally, i

This compound is primarily utilized in organic synthesis as a versatile intermediate for constructing complex aromatic structures. Its functional groups, including bromo, chloromethyl, and iodo substituents, make it highly reactive in cross-coupling reactions, such as Suzuki or Sonogashira couplings, enabling the formation of carbon-carbon bonds. It is also employed in the preparation of pharmaceuticals and agrochemicals, where its halogenated aromatic core serves as a key building block. Additionally, its reactivity allows for further functionalization, making it valuable in material science for developing advanced polymers or organic electronic materials.

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