3-Bromo-4,5-dimethylpyridine

98%

Reagent Code: #146853
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CAS Number 27063-98-5

science Other reagents with same CAS 27063-98-5

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Weight 186.05 g/mol
Formula C₇H₈BrN
inventory_2 Storage & Handling
Storage Room temperature, dry

description Product Description

Used in the synthesis of pharmaceutical intermediates, particularly in the development of nicotinic receptor modulators. Serves as a building block in agrochemicals for creating herbicides and insecticides due to its reactive bromine site enabling cross-coupling reactions. Employed in research laboratories for constructing complex pyridine-based structures in medicinal chemistry. Its methyl groups enhance lipophilicity, improving cell membrane permeability in drug design. Commonly utilized in Suzuki and Negishi coupling reactions to form carbon-carbon bonds in advanced organic synthesis.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,260.00
inventory 250mg
10-20 days ฿2,170.00
inventory 1g
10-20 days ฿8,570.00
inventory 5g
10-20 days ฿37,170.00

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3-Bromo-4,5-dimethylpyridine
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Used in the synthesis of pharmaceutical intermediates, particularly in the development of nicotinic receptor modulators. Serves as a building block in agrochemicals for creating herbicides and insecticides due to its reactive bromine site enabling cross-coupling reactions. Employed in research laboratories for constructing complex pyridine-based structures in medicinal chemistry. Its methyl groups enhance lipophilicity, improving cell membrane permeability in drug design. Commonly utilized in Suzuki and

Used in the synthesis of pharmaceutical intermediates, particularly in the development of nicotinic receptor modulators. Serves as a building block in agrochemicals for creating herbicides and insecticides due to its reactive bromine site enabling cross-coupling reactions. Employed in research laboratories for constructing complex pyridine-based structures in medicinal chemistry. Its methyl groups enhance lipophilicity, improving cell membrane permeability in drug design. Commonly utilized in Suzuki and Negishi coupling reactions to form carbon-carbon bonds in advanced organic synthesis.

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