5-Bromo-2-chloro-3-(difluoromethyl)pyridine

98%

Reagent Code: #152502
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CAS Number 1332392-76-3

science Other reagents with same CAS 1332392-76-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 242.45 g/mol
Formula C₆H₃BrClF₂N
badge Registry Numbers
MDL Number MFCD22199307
inventory_2 Storage & Handling
Storage 2-8°C, Inert Gas

description Product Description

Used as a key intermediate in the synthesis of agrochemicals, particularly in the development of herbicides and insecticides. Its structure allows for selective reactivity, making it valuable in creating active ingredients that target specific pests while minimizing environmental impact. Also employed in pharmaceutical research for building blocks in heterocyclic compounds, especially in candidates for antiparasitic and anti-inflammatory drugs. The halogen substituents enable cross-coupling reactions, facilitating the construction of complex molecules in drug discovery and crop protection chemistry.

Available Sizes & Pricing

Size Availability Unit Price Quantity
100mg
10-20 days ฿1,810.00
250mg
10-20 days ฿4,170.00
1g
10-20 days ฿15,620.00
5g
10-20 days ฿67,790.00
5-Bromo-2-chloro-3-(difluoromethyl)pyridine
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Used as a key intermediate in the synthesis of agrochemicals, particularly in the development of herbicides and insecticides. Its structure allows for selective reactivity, making it valuable in creating active ingredients that target specific pests while minimizing environmental impact. Also employed in pharmaceutical research for building blocks in heterocyclic compounds, especially in candidates for antiparasitic and anti-inflammatory drugs. The halogen substituents enable cross-coupling reactions, facil
Used as a key intermediate in the synthesis of agrochemicals, particularly in the development of herbicides and insecticides. Its structure allows for selective reactivity, making it valuable in creating active ingredients that target specific pests while minimizing environmental impact. Also employed in pharmaceutical research for building blocks in heterocyclic compounds, especially in candidates for antiparasitic and anti-inflammatory drugs. The halogen substituents enable cross-coupling reactions, facilitating the construction of complex molecules in drug discovery and crop protection chemistry.
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