3-Bromo-2-(trifluoromethyl)pyridine

98%

Reagent Code: #144500
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CAS Number 590371-58-7

science Other reagents with same CAS 590371-58-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 225.99 g/mol
Formula C₆H₃BrF₃N
badge Registry Numbers
MDL Number MFCD08458124
thermostat Physical Properties
Melting Point 34-36 °C
Boiling Point 165.2°C at 760 mmHg
inventory_2 Storage & Handling
Storage Room temperature, dry, sealed

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of herbicides and fungicides. Its structure allows for selective functionalization, making it valuable in creating active ingredients with improved efficacy and environmental profiles. Commonly employed in cross-coupling reactions, such as Suzuki and Negishi couplings, to build complex molecules in medicinal chemistry. Also utilized in the production of specialty chemicals where halogen and trifluoromethyl groups enhance biological activity or stability.

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Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿2,850.00
inventory 10g
10-20 days ฿5,400.00
inventory 25g
10-20 days ฿13,480.00

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3-Bromo-2-(trifluoromethyl)pyridine
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Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of herbicides and fungicides. Its structure allows for selective functionalization, making it valuable in creating active ingredients with improved efficacy and environmental profiles. Commonly employed in cross-coupling reactions, such as Suzuki and Negishi couplings, to build complex molecules in medicinal chemistry. Also utilized in the production of specialty chemicals where halogen and trif
Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of herbicides and fungicides. Its structure allows for selective functionalization, making it valuable in creating active ingredients with improved efficacy and environmental profiles. Commonly employed in cross-coupling reactions, such as Suzuki and Negishi couplings, to build complex molecules in medicinal chemistry. Also utilized in the production of specialty chemicals where halogen and trifluoromethyl groups enhance biological activity or stability.
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