5-bromo-4-chloropyridin-2-amine

≥95%

Reagent Code: #144074
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CAS Number 942947-94-6

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Weight 207.46 g/mol
Formula C₅H₄BrClN₂
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MDL Number MFCD12407282
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Storage Room temperature

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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors for cancer treatment. It serves as a building block in agrochemicals, contributing to the creation of herbicides and pesticides due to its ability to enhance bioactivity. Its halogenated pyridine structure allows for selective functionalization, making it valuable in medicinal chemistry for structure-activity relationship studies. Also employed in the preparation of dyes and functional materials where nitrogen-containing heterocycles improve stability and electronic properties.

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Size Availability Unit Price Quantity
inventory 10g
10-20 days ฿1,360.00
inventory 100g
10-20 days ฿10,530.00
inventory 500g
10-20 days ฿47,830.00
inventory 25g
10-20 days ฿3,400.00

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5-bromo-4-chloropyridin-2-amine
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors for cancer treatment. It serves as a building block in agrochemicals, contributing to the creation of herbicides and pesticides due to its ability to enhance bioactivity. Its halogenated pyridine structure allows for selective functionalization, making it valuable in medicinal chemistry for structure-activity relationship studies. Also employed in the preparation of dyes and functional mat

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors for cancer treatment. It serves as a building block in agrochemicals, contributing to the creation of herbicides and pesticides due to its ability to enhance bioactivity. Its halogenated pyridine structure allows for selective functionalization, making it valuable in medicinal chemistry for structure-activity relationship studies. Also employed in the preparation of dyes and functional materials where nitrogen-containing heterocycles improve stability and electronic properties.

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