4-Bromo-2,6-dichloropyridine

97%

Reagent Code: #69826
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CAS Number 98027-80-6

science Other reagents with same CAS 98027-80-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 226.89 g/mol
Formula C₅H₂BrCl₂N
badge Registry Numbers
MDL Number MFCD11848646
inventory_2 Storage & Handling
Storage room temperature, dry

description Product Description

Used in organic synthesis as a building block for creating complex molecules, particularly in pharmaceuticals and agrochemicals. It serves as an intermediate in the production of active ingredients for drugs, including antiviral and antifungal agents. Additionally, it is employed in the development of herbicides and pesticides due to its structural properties that enhance target specificity. Its halogenated structure makes it valuable in cross-coupling reactions, such as Suzuki and Buchwald-Hartwig reactions, which are crucial in medicinal chemistry.

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Test Parameter Specification
Appearance White to yellow solid
Purity 96.5-100
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

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Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿6,280.00
inventory 1g
10-20 days ฿1,760.00

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4-Bromo-2,6-dichloropyridine
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Used in organic synthesis as a building block for creating complex molecules, particularly in pharmaceuticals and agrochemicals. It serves as an intermediate in the production of active ingredients for drugs, including antiviral and antifungal agents. Additionally, it is employed in the development of herbicides and pesticides due to its structural properties that enhance target specificity. Its halogenated structure makes it valuable in cross-coupling reactions, such as Suzuki and Buchwald-Hartwig react

Used in organic synthesis as a building block for creating complex molecules, particularly in pharmaceuticals and agrochemicals. It serves as an intermediate in the production of active ingredients for drugs, including antiviral and antifungal agents. Additionally, it is employed in the development of herbicides and pesticides due to its structural properties that enhance target specificity. Its halogenated structure makes it valuable in cross-coupling reactions, such as Suzuki and Buchwald-Hartwig reactions, which are crucial in medicinal chemistry.

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