2-Bromo-4-iodobenzamide

97%

Reagent Code: #148601
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CAS Number 1261516-26-0

science Other reagents with same CAS 1261516-26-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 325.93 g/mol
Formula C₇H₅BrINO
badge Registry Numbers
MDL Number MFCD18391622
inventory_2 Storage & Handling
Storage Room temperature, dry and sealed from light

description Product Description

Used primarily as an intermediate in organic synthesis, especially in pharmaceutical and agrochemical industries. It serves as a building block in the preparation of bioactive molecules due to the presence of both bromo and iodo functional groups, which are amenable to cross-coupling reactions such as Suzuki, Stille, and Heck reactions. Its amide group allows for hydrogen bonding and polarity, making it useful in the development of compounds with specific biological activity. Commonly employed in the synthesis of potential drug candidates, including kinase inhibitors and anti-inflammatory agents. Also utilized in research settings for the construction of complex aromatic structures and labeled compounds.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,950.00
inventory 250mg
10-20 days ฿3,310.00
inventory 1g
10-20 days ฿13,170.00
inventory 5g
10-20 days ฿32,570.00
inventory 10g
10-20 days ฿57,620.00

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2-Bromo-4-iodobenzamide
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Used primarily as an intermediate in organic synthesis, especially in pharmaceutical and agrochemical industries. It serves as a building block in the preparation of bioactive molecules due to the presence of both bromo and iodo functional groups, which are amenable to cross-coupling reactions such as Suzuki, Stille, and Heck reactions. Its amide group allows for hydrogen bonding and polarity, making it useful in the development of compounds with specific biological activity. Commonly employed in the syn

Used primarily as an intermediate in organic synthesis, especially in pharmaceutical and agrochemical industries. It serves as a building block in the preparation of bioactive molecules due to the presence of both bromo and iodo functional groups, which are amenable to cross-coupling reactions such as Suzuki, Stille, and Heck reactions. Its amide group allows for hydrogen bonding and polarity, making it useful in the development of compounds with specific biological activity. Commonly employed in the synthesis of potential drug candidates, including kinase inhibitors and anti-inflammatory agents. Also utilized in research settings for the construction of complex aromatic structures and labeled compounds.

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