2-Bromo-4,6-dimethylpyridin-3-amine

95%

Reagent Code: #145313
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CAS Number 104829-98-3

science Other reagents with same CAS 104829-98-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 201.06 g/mol
Formula C₇H₉BrN₂
badge Registry Numbers
MDL Number MFCD03731181
thermostat Physical Properties
Boiling Point 304.8°C
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and other biologically active compounds. The 3-amino and 2-bromo substituents on the 4,6-dimethylpyridine ring allow for selective functionalization, making it valuable in medicinal chemistry for creating analogs with potential anti-inflammatory, anticancer, or antimicrobial properties. Commonly employed in cross-coupling reactions such as Suzuki or Buchwald-Hartwig aminations to build complex heterocyclic systems found in drug candidates. Also utilized in agrochemical research for designing novel pesticides and herbicides due to its stability and reactivity profile.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿990.00
inventory 1g
10-20 days ฿2,650.00
inventory 5g
10-20 days ฿11,290.00
inventory 25g
10-20 days ฿36,500.00

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2-Bromo-4,6-dimethylpyridin-3-amine
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and other biologically active compounds. The 3-amino and 2-bromo substituents on the 4,6-dimethylpyridine ring allow for selective functionalization, making it valuable in medicinal chemistry for creating analogs with potential anti-inflammatory, anticancer, or antimicrobial properties. Commonly employed in cross-coupling reactions such as Suzuki or Buchwald-Hartwig aminations to build com

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and other biologically active compounds. The 3-amino and 2-bromo substituents on the 4,6-dimethylpyridine ring allow for selective functionalization, making it valuable in medicinal chemistry for creating analogs with potential anti-inflammatory, anticancer, or antimicrobial properties. Commonly employed in cross-coupling reactions such as Suzuki or Buchwald-Hartwig aminations to build complex heterocyclic systems found in drug candidates. Also utilized in agrochemical research for designing novel pesticides and herbicides due to its stability and reactivity profile.

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