4-methyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-2-(methylsulfonyl)pyridine

≥95%

Reagent Code: #205732
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CAS Number 1353745-98-8

science Other reagents with same CAS 1353745-98-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 297.18 g/mol
Formula C₁₃H₂₀BNO₄S
badge Registry Numbers
MDL Number MFCD18727629
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Widely used in Suzuki-Miyaura cross-coupling reactions, this compound serves as a key boronic ester reagent in the synthesis of pharmaceutical intermediates and functionalized pyridine derivatives. Its boron-containing group enables efficient carbon-carbon bond formation under mild palladium catalysis, making it valuable in drug discovery and development. The methylsulfonyl group enhances reactivity and directs further functionalization, allowing selective construction of complex molecules. It is particularly useful in preparing bioactive compounds, including kinase inhibitors and other therapeutic agents. Its stability and reactivity profile make it suitable for automated synthesis and high-throughput screening in medicinal chemistry.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿13,830.00
inventory 250mg
10-20 days ฿23,510.00
inventory 1g
10-20 days ฿77,870.00
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4-methyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-2-(methylsulfonyl)pyridine
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Widely used in Suzuki-Miyaura cross-coupling reactions, this compound serves as a key boronic ester reagent in the synthesis of pharmaceutical intermediates and functionalized pyridine derivatives. Its boron-containing group enables efficient carbon-carbon bond formation under mild palladium catalysis, making it valuable in drug discovery and development. The methylsulfonyl group enhances reactivity and directs further functionalization, allowing selective construction of complex molecules. It is particu

Widely used in Suzuki-Miyaura cross-coupling reactions, this compound serves as a key boronic ester reagent in the synthesis of pharmaceutical intermediates and functionalized pyridine derivatives. Its boron-containing group enables efficient carbon-carbon bond formation under mild palladium catalysis, making it valuable in drug discovery and development. The methylsulfonyl group enhances reactivity and directs further functionalization, allowing selective construction of complex molecules. It is particularly useful in preparing bioactive compounds, including kinase inhibitors and other therapeutic agents. Its stability and reactivity profile make it suitable for automated synthesis and high-throughput screening in medicinal chemistry.

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