2-Bromo-6-phenoxypyridine

95%

Reagent Code: #149026
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CAS Number 83247-00-1

science Other reagents with same CAS 83247-00-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 250.09 g/mol
Formula C₁₁H₈BrNO
badge Registry Numbers
MDL Number MFCD01646084
thermostat Physical Properties
Melting Point 83-86 °C
Boiling Point 327.2±27.0 °C at 760 mmHg
inventory_2 Storage & Handling
Density 1.476±0.06 g/cm3
Storage 2-8°C, dry

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of herbicides and plant growth regulators. It serves as a building block in the preparation of more complex pyridine derivatives with biological activity. Commonly employed in cross-coupling reactions, such as Suzuki or Heck reactions, to form carbon-carbon bonds in the production of active ingredients in crop protection agents. Also utilized in research for developing new kinase inhibitors and other bioactive molecules in medicinal chemistry.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿4,800.00
inventory 250mg
10-20 days ฿8,000.00
inventory 1g
10-20 days ฿12,800.00
inventory 5g
10-20 days ฿38,400.00

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2-Bromo-6-phenoxypyridine
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Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of herbicides and plant growth regulators. It serves as a building block in the preparation of more complex pyridine derivatives with biological activity. Commonly employed in cross-coupling reactions, such as Suzuki or Heck reactions, to form carbon-carbon bonds in the production of active ingredients in crop protection agents. Also utilized in research for developing new kinase inhibitors and

Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of herbicides and plant growth regulators. It serves as a building block in the preparation of more complex pyridine derivatives with biological activity. Commonly employed in cross-coupling reactions, such as Suzuki or Heck reactions, to form carbon-carbon bonds in the production of active ingredients in crop protection agents. Also utilized in research for developing new kinase inhibitors and other bioactive molecules in medicinal chemistry.

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