2-Bromo-4-chloro-5-iodopyridine

≥95%

Reagent Code: #43237
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CAS Number 1364663-37-5

science Other reagents with same CAS 1364663-37-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 318.34 g/mol
Formula C₅H₂BrClIN
badge Registry Numbers
MDL Number MFCD22199250
thermostat Physical Properties
Boiling Point 304.4±37.0°C at 760 mmHg
inventory_2 Storage & Handling
Storage -20°C, protected from light and stored in an inert gas

description Product Description

This chemical is primarily utilized in organic synthesis as a versatile building block for the development of more complex molecules. Its unique halogen substitution pattern makes it valuable in cross-coupling reactions, such as Suzuki or Sonogashira couplings, to create substituted pyridine derivatives. These derivatives are often explored for their potential in pharmaceutical research, particularly in the design of drug candidates targeting various diseases. Additionally, it serves as a key intermediate in the synthesis of agrochemicals and materials with specific electronic properties. Its reactivity allows for selective functionalization, enabling researchers to tailor compounds for specific applications in medicinal chemistry and material science.

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Test Parameter Specification
Appearance Off-white to yellow solid
Purity (%) 94.5-100%
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿8,082.00
inventory 5g
10-20 days ฿39,951.00
inventory 250mg
10-20 days ฿2,502.00
inventory 100mg
10-20 days ฿1,152.00

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2-Bromo-4-chloro-5-iodopyridine
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This chemical is primarily utilized in organic synthesis as a versatile building block for the development of more complex molecules. Its unique halogen substitution pattern makes it valuable in cross-coupling reactions, such as Suzuki or Sonogashira couplings, to create substituted pyridine derivatives. These derivatives are often explored for their potential in pharmaceutical research, particularly in the design of drug candidates targeting various diseases. Additionally, it serves as a key intermediat

This chemical is primarily utilized in organic synthesis as a versatile building block for the development of more complex molecules. Its unique halogen substitution pattern makes it valuable in cross-coupling reactions, such as Suzuki or Sonogashira couplings, to create substituted pyridine derivatives. These derivatives are often explored for their potential in pharmaceutical research, particularly in the design of drug candidates targeting various diseases. Additionally, it serves as a key intermediate in the synthesis of agrochemicals and materials with specific electronic properties. Its reactivity allows for selective functionalization, enabling researchers to tailor compounds for specific applications in medicinal chemistry and material science.

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