4-Bromo-2-(Difluoromethoxy)-6-Methylpyridine

97%

Reagent Code: #154070
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CAS Number 1227184-58-8

science Other reagents with same CAS 1227184-58-8

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Weight 238.03 g/mol
Formula C₇H₆BrF₂NO
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as a key intermediate in the synthesis of agrochemicals and pharmaceuticals, particularly in the development of herbicides and fungicides. Its structure allows for selective substitution reactions, making it valuable in creating active ingredients with improved efficacy and environmental profiles. Commonly employed in cross-coupling reactions such as Suzuki or Buchwald-Hartwig aminations to build complex molecules. Also utilized in research for novel drug candidates targeting central nervous system disorders due to its ability to cross biological membranes and interact with specific enzyme sites.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿8,210.00
inventory 250mg
10-20 days ฿16,750.00

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4-Bromo-2-(Difluoromethoxy)-6-Methylpyridine
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Used as a key intermediate in the synthesis of agrochemicals and pharmaceuticals, particularly in the development of herbicides and fungicides. Its structure allows for selective substitution reactions, making it valuable in creating active ingredients with improved efficacy and environmental profiles. Commonly employed in cross-coupling reactions such as Suzuki or Buchwald-Hartwig aminations to build complex molecules. Also utilized in research for novel drug candidates targeting central nervous system

Used as a key intermediate in the synthesis of agrochemicals and pharmaceuticals, particularly in the development of herbicides and fungicides. Its structure allows for selective substitution reactions, making it valuable in creating active ingredients with improved efficacy and environmental profiles. Commonly employed in cross-coupling reactions such as Suzuki or Buchwald-Hartwig aminations to build complex molecules. Also utilized in research for novel drug candidates targeting central nervous system disorders due to its ability to cross biological membranes and interact with specific enzyme sites.

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