1,3-Dibromo-5-fluorobenzene

98%

Reagent Code: #114136
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CAS Number 1435-51-4

science Other reagents with same CAS 1435-51-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 253.89 g/mol
Formula C₆H₃Br₂F
badge Registry Numbers
MDL Number MFCD00061119
thermostat Physical Properties
Boiling Point 204-206 °C768 mm Hg(lit.)
inventory_2 Storage & Handling
Density 2.018 g/mL at 25 °C(lit.)
Storage room temperature

description Product Description

1,3-Dibromo-5-fluorobenzene is primarily used as an intermediate in organic synthesis. It plays a key role in the production of pharmaceuticals, where it serves as a building block for more complex molecules. The compound is also utilized in the development of agrochemicals, contributing to the creation of herbicides and pesticides. Additionally, it finds application in material science, particularly in the synthesis of specialty polymers and advanced materials. Its unique halogenated structure makes it valuable for cross-coupling reactions in organic chemistry, enabling the formation of carbon-carbon and carbon-heteroatom bonds.

format_list_bulleted Product Specification

Test Parameter Specification
Purity (GC) 98-100
Refractive Index (N20/D) 1.576-1.58
Relative Density (20/20) 2.024-2.028
Appearance Colorless to light yellow liquid
Infrared Spectrum Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿380.00
inventory 25g
10-20 days ฿1,290.00
inventory 100g
10-20 days ฿4,960.00

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1,3-Dibromo-5-fluorobenzene
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1,3-Dibromo-5-fluorobenzene is primarily used as an intermediate in organic synthesis. It plays a key role in the production of pharmaceuticals, where it serves as a building block for more complex molecules. The compound is also utilized in the development of agrochemicals, contributing to the creation of herbicides and pesticides. Additionally, it finds application in material science, particularly in the synthesis of specialty polymers and advanced materials. Its unique halogenated structure makes it valuable for cross-coupling reactions in organic chemistry, enabling the formation of carbon-carbon and carbon-heteroatom bonds.
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