2-Bromo-6-iodopyridin-3-ol

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Reagent Code: #85190
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CAS Number 129611-32-1

science Other reagents with same CAS 129611-32-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 299.89 g/mol
Formula C₅H₃BrINO
badge Registry Numbers
MDL Number MFCD09909342
thermostat Physical Properties
Melting Point 141-142 °C(Solv: chloroform (67-66-3))
Boiling Point 404°C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, protected from light, stored in an inert gas

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of complex organic compounds. It plays a role in the preparation of pyridine derivatives, which are essential in drug discovery and medicinal chemistry. The compound is also utilized in cross-coupling reactions, such as Suzuki and Heck reactions, to create biologically active molecules. Its halogenated structure makes it valuable for constructing heterocyclic frameworks in agrochemicals and fine chemicals. Additionally, it is employed in research for designing ligands and catalysts in organic synthesis.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿603.00
inventory 1g
10-20 days ฿1,368.00
inventory 5g
10-20 days ฿5,256.00
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2-Bromo-6-iodopyridin-3-ol
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Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of complex organic compounds. It plays a role in the preparation of pyridine derivatives, which are essential in drug discovery and medicinal chemistry. The compound is also utilized in cross-coupling reactions, such as Suzuki and Heck reactions, to create biologically active molecules. Its halogenated structure makes it valuable for constructing heterocyclic frameworks in agrochemicals and fine chemicals. Additi

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of complex organic compounds. It plays a role in the preparation of pyridine derivatives, which are essential in drug discovery and medicinal chemistry. The compound is also utilized in cross-coupling reactions, such as Suzuki and Heck reactions, to create biologically active molecules. Its halogenated structure makes it valuable for constructing heterocyclic frameworks in agrochemicals and fine chemicals. Additionally, it is employed in research for designing ligands and catalysts in organic synthesis.

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