4-Bromo-2-(1-hydroxyethyl)pyridine

95%

Reagent Code: #144661
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CAS Number 1471260-48-6

science Other reagents with same CAS 1471260-48-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 202.05 g/mol
Formula C₇H₈BrNO
badge Registry Numbers
MDL Number MFCD28131961
inventory_2 Storage & Handling
Storage Room temperature, seal, dry

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of central nervous system agents and kinase inhibitors. Its structure allows for selective functionalization, making it valuable in creating biologically active compounds. Commonly employed in cross-coupling reactions such as Suzuki or Heck reactions to build complex heterocyclic systems. Also utilized in agrochemical research for designing novel active ingredients. The hydroxyethyl group enables further derivatization, enhancing its utility in medicinal chemistry.

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Test Parameter Specification
Purity 95-100
Appearance White to pale yellow crystals or powder

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿9,450.00

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4-Bromo-2-(1-hydroxyethyl)pyridine
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Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of central nervous system agents and kinase inhibitors. Its structure allows for selective functionalization, making it valuable in creating biologically active compounds. Commonly employed in cross-coupling reactions such as Suzuki or Heck reactions to build complex heterocyclic systems. Also utilized in agrochemical research for designing novel active ingredients. The hydroxyethyl group enables further derivati

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of central nervous system agents and kinase inhibitors. Its structure allows for selective functionalization, making it valuable in creating biologically active compounds. Commonly employed in cross-coupling reactions such as Suzuki or Heck reactions to build complex heterocyclic systems. Also utilized in agrochemical research for designing novel active ingredients. The hydroxyethyl group enables further derivatization, enhancing its utility in medicinal chemistry.

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