(4-bromo-2-iodophenyl)methanol

99%

Reagent Code: #149220
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CAS Number 1261438-69-0

science Other reagents with same CAS 1261438-69-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 312.93 g/mol
Formula C₇H₆BrIO
inventory_2 Storage & Handling
Storage 2-8℃

description Product Description

Used primarily as a key intermediate in the synthesis of pharmaceuticals and agrochemicals. Its structure allows for selective cross-coupling reactions, making it valuable in the development of complex organic molecules. Commonly employed in the preparation of bioactive compounds, especially in the construction of aryl-aryl and aryl-heteroaryl bonds via palladium-catalyzed reactions. Also utilized in the manufacture of certain specialty dyes and fluorescent probes due to its halogen substitution pattern, which facilitates further functionalization. Its hydroxyl group enables esterification or ether formation, expanding its utility in medicinal chemistry for building molecular diversity.

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Test Parameter Specification
Appearance off-white solid
Purity (%) 99-100%
Infrared Spectrum Conforms to Structure

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Size Availability Unit Price Quantity
inventory 500mg
10-20 days ฿3,186.00
inventory 1g
10-20 days ฿4,968.00
inventory 5g
10-20 days ฿15,012.00

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(4-bromo-2-iodophenyl)methanol
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Used primarily as a key intermediate in the synthesis of pharmaceuticals and agrochemicals. Its structure allows for selective cross-coupling reactions, making it valuable in the development of complex organic molecules. Commonly employed in the preparation of bioactive compounds, especially in the construction of aryl-aryl and aryl-heteroaryl bonds via palladium-catalyzed reactions. Also utilized in the manufacture of certain specialty dyes and fluorescent probes due to its halogen substitution pattern,

Used primarily as a key intermediate in the synthesis of pharmaceuticals and agrochemicals. Its structure allows for selective cross-coupling reactions, making it valuable in the development of complex organic molecules. Commonly employed in the preparation of bioactive compounds, especially in the construction of aryl-aryl and aryl-heteroaryl bonds via palladium-catalyzed reactions. Also utilized in the manufacture of certain specialty dyes and fluorescent probes due to its halogen substitution pattern, which facilitates further functionalization. Its hydroxyl group enables esterification or ether formation, expanding its utility in medicinal chemistry for building molecular diversity.

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