4-bromo-3,5-dimethylpyridine hydrochloride

≥95%

Reagent Code: #143922
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CAS Number 201286-65-9

science Other reagents with same CAS 201286-65-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 222.51 g/mol
Formula C₇H₉BrClN
badge Registry Numbers
MDL Number MFCD12922840
inventory_2 Storage & Handling
Storage Room temperature

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. Its structure allows for selective functionalization, making it valuable in medicinal chemistry for creating targeted drug candidates. Commonly employed in cross-coupling reactions such as Suzuki or Buchwald-Hartwig aminations to build complex heterocyclic systems. Also utilized in agrochemical research for designing new active ingredients in crop protection agents. The hydrochloride salt form enhances stability and solubility, facilitating handling and reaction efficiency in various synthetic pathways.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿2,320.00
inventory 250mg
10-20 days ฿5,120.00
inventory 5g
10-20 days ฿36,800.00
inventory 1g
10-20 days ฿12,800.00

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4-bromo-3,5-dimethylpyridine hydrochloride
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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. Its structure allows for selective functionalization, making it valuable in medicinal chemistry for creating targeted drug candidates. Commonly employed in cross-coupling reactions such as Suzuki or Buchwald-Hartwig aminations to build complex heterocyclic systems. Also utilized in agrochemical research for designing new active ingredients in crop p

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and other biologically active compounds. Its structure allows for selective functionalization, making it valuable in medicinal chemistry for creating targeted drug candidates. Commonly employed in cross-coupling reactions such as Suzuki or Buchwald-Hartwig aminations to build complex heterocyclic systems. Also utilized in agrochemical research for designing new active ingredients in crop protection agents. The hydrochloride salt form enhances stability and solubility, facilitating handling and reaction efficiency in various synthetic pathways.

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