2-(2-Fluoro-3-methylphenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

97%

Reagent Code: #115616
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CAS Number 1192548-08-5

science Other reagents with same CAS 1192548-08-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 236.09 g/mol
Formula C₁₃H₁₈BFO₂
badge Registry Numbers
MDL Number MFCD18384075
thermostat Physical Properties
Boiling Point 308.5±35.0°C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, store under inert gas

description Product Description

This chemical is primarily used in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura reactions. It serves as a boronic ester reagent, enabling the formation of carbon-carbon bonds in the production of complex organic molecules. Its application is significant in pharmaceutical research and development, where it aids in the synthesis of drug candidates and bioactive compounds. Additionally, it is utilized in material science for creating advanced polymers and functional materials. The fluorine and methyl groups on the phenyl ring enhance its reactivity and selectivity in various chemical transformations.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿396.00
inventory 1g
10-20 days ฿891.00
inventory 5g
10-20 days ฿3,573.00

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2-(2-Fluoro-3-methylphenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
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This chemical is primarily used in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura reactions. It serves as a boronic ester reagent, enabling the formation of carbon-carbon bonds in the production of complex organic molecules. Its application is significant in pharmaceutical research and development, where it aids in the synthesis of drug candidates and bioactive compounds. Additionally, it is utilized in material science for creating advanced polymers and functional mat

This chemical is primarily used in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura reactions. It serves as a boronic ester reagent, enabling the formation of carbon-carbon bonds in the production of complex organic molecules. Its application is significant in pharmaceutical research and development, where it aids in the synthesis of drug candidates and bioactive compounds. Additionally, it is utilized in material science for creating advanced polymers and functional materials. The fluorine and methyl groups on the phenyl ring enhance its reactivity and selectivity in various chemical transformations.

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