2-(4-Methoxy-3-nitrophenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

96%

Reagent Code: #212192
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CAS Number 554411-20-0

science Other reagents with same CAS 554411-20-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 279.1 g/mol
Formula C₁₃H₁₈BNO₅
badge Registry Numbers
MDL Number MFCD06795663
inventory_2 Storage & Handling
Storage 2-8°C, dry

description Product Description

Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in the synthesis of complex organic molecules. Its boronate ester group facilitates palladium-catalyzed coupling with aryl halides, making it valuable in pharmaceutical and agrochemical research for constructing biaryl scaffolds. The methoxy and nitro substituents provide sites for further functionalization or act as directing groups in synthesis. Stable and easy to handle, it supports efficient and selective transformations in modern organic chemistry workflows.

Available Sizes & Pricing

Size Availability Unit Price Quantity
250mg
10-20 days ฿2,160.00
1g
10-20 days ฿5,720.00
5g
10-20 days ฿20,270.00
10g
10-20 days ฿36,670.00
2-(4-Methoxy-3-nitrophenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
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Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in the synthesis of complex organic molecules. Its boronate ester group facilitates palladium-catalyzed coupling with aryl halides, making it valuable in pharmaceutical and agrochemical research for constructing biaryl scaffolds. The methoxy and nitro substituents provide sites for further functionalization or act as directing groups in synthesis. Stable and easy to handle, it supports efficient and selective transformations in modern organic chemistry workflows.
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