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.

Available Sizes & Pricing

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