4-Iodophenylboronic acid

98%

Reagent Code: #90711
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Alias p-Iodophenylboronic acid
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CAS Number 5122-99-6

science Other reagents with same CAS 5122-99-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 247.83 g/mol
Formula C₆H₆BIO₂
badge Registry Numbers
MDL Number MFCD01319014
thermostat Physical Properties
Melting Point 326-330 °C
inventory_2 Storage & Handling
Storage 2~8°C

description Product Description

This compound is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, where it serves as a key building block for creating biaryl structures. These reactions are essential in the production of pharmaceuticals, agrochemicals, and advanced materials. Additionally, it is utilized in the development of sensors and probes due to its ability to interact with diols and sugars, making it valuable in biochemical and diagnostic applications. Its iodine substituent also allows for further functionalization, enhancing its versatility in synthetic chemistry.

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Test Parameter Specification
Purity 98-100%
Melting Point 326-330
Appearance White to off-white powder

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿400.00
inventory 5g
10-20 days ฿1,760.00
inventory 25g
10-20 days ฿8,230.00

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4-Iodophenylboronic acid
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This compound is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, where it serves as a key building block for creating biaryl structures. These reactions are essential in the production of pharmaceuticals, agrochemicals, and advanced materials. Additionally, it is utilized in the development of sensors and probes due to its ability to interact with diols and sugars, making it valuable in biochemical and diagnostic applications. Its iodine substituent also allows

This compound is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, where it serves as a key building block for creating biaryl structures. These reactions are essential in the production of pharmaceuticals, agrochemicals, and advanced materials. Additionally, it is utilized in the development of sensors and probes due to its ability to interact with diols and sugars, making it valuable in biochemical and diagnostic applications. Its iodine substituent also allows for further functionalization, enhancing its versatility in synthetic chemistry.

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