2-(3-Fluoro-4-((methylsulfonyl)methyl)phenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

95%

Reagent Code: #188844
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CAS Number 1351499-67-6

science Other reagents with same CAS 1351499-67-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 314.18 g/mol
Formula C₁₄H₂₀BFO₄S
badge Registry Numbers
MDL Number MFCD18760488
inventory_2 Storage & Handling
Storage Room temperature, sealed

description Product Description

Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions, this compound enables the formation of carbon-carbon bonds in the synthesis of complex organic molecules. Its primary application lies in pharmaceutical and agrochemical research, where it serves as a building block for introducing aromatic and fluorinated moieties into target structures. The presence of the methylsulfonyl group enhances reactivity and selectivity in coupling processes, making it valuable for developing bioactive compounds. Additionally, its boronate ester functionality allows for mild and efficient transformations under palladium catalysis, supporting its use in late-stage functionalization during drug discovery.

Available Sizes & Pricing

Size Availability Unit Price Quantity
100mg
10-20 days ฿2,840.00
250mg
10-20 days ฿4,820.00
1g
10-20 days ฿13,000.00
5g
10-20 days ฿45,500.00
2-(3-Fluoro-4-((methylsulfonyl)methyl)phenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
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Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions, this compound enables the formation of carbon-carbon bonds in the synthesis of complex organic molecules. Its primary application lies in pharmaceutical and agrochemical research, where it serves as a building block for introducing aromatic and fluorinated moieties into target structures. The presence of the methylsulfonyl group enhances reactivity and selectivity in coupling processes, making it valuable for developing bioactive compounds. Additionally, its boronate ester functionality allows for mild and efficient transformations under palladium catalysis, supporting its use in late-stage functionalization during drug discovery.
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