(2-Bromo-3-iodophenyl)methanamine

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Reagent Code: #113121
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CAS Number 1261448-43-4

science Other reagents with same CAS 1261448-43-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 311.95 g/mol
Formula C₇H₇BrIN
badge Registry Numbers
MDL Number MFCD18391658
inventory_2 Storage & Handling
Storage 2-8°C, protected from light, stored in an inert gas

description Product Description

This chemical is primarily utilized in organic synthesis, particularly in the development of complex molecules for pharmaceutical research. It serves as a key intermediate in the creation of various biologically active compounds, including potential drug candidates. The presence of both bromine and iodine atoms on the aromatic ring makes it a versatile building block for further functionalization through cross-coupling reactions, such as Suzuki or Sonogashira reactions. Additionally, its amine group allows for further derivatization, enabling the synthesis of amides, imines, or other nitrogen-containing structures. This compound is particularly valuable in medicinal chemistry for designing molecules with specific target interactions, such as enzyme inhibitors or receptor modulators. Its unique structure also makes it useful in material science for developing organic electronic materials or ligands in coordination chemistry.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿7,461.00
inventory 250mg
10-20 days ฿14,913.00

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(2-Bromo-3-iodophenyl)methanamine
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This chemical is primarily utilized in organic synthesis, particularly in the development of complex molecules for pharmaceutical research. It serves as a key intermediate in the creation of various biologically active compounds, including potential drug candidates. The presence of both bromine and iodine atoms on the aromatic ring makes it a versatile building block for further functionalization through cross-coupling reactions, such as Suzuki or Sonogashira reactions. Additionally, its amine group allo

This chemical is primarily utilized in organic synthesis, particularly in the development of complex molecules for pharmaceutical research. It serves as a key intermediate in the creation of various biologically active compounds, including potential drug candidates. The presence of both bromine and iodine atoms on the aromatic ring makes it a versatile building block for further functionalization through cross-coupling reactions, such as Suzuki or Sonogashira reactions. Additionally, its amine group allows for further derivatization, enabling the synthesis of amides, imines, or other nitrogen-containing structures. This compound is particularly valuable in medicinal chemistry for designing molecules with specific target interactions, such as enzyme inhibitors or receptor modulators. Its unique structure also makes it useful in material science for developing organic electronic materials or ligands in coordination chemistry.

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