tert-Butyl 3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzoate

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Reagent Code: #145932
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CAS Number 903895-48-7

science Other reagents with same CAS 903895-48-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 304.19 g/mol
Formula C₁₇H₂₅BO₄
badge Registry Numbers
MDL Number MFCD03453057
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 for forming carbon-carbon bonds in organic synthesis. Its stability and reactivity make it valuable for constructing biaryl and aryl systems found in pharmaceuticals, agrochemicals, and advanced materials. The tert-butyl ester group remains intact under typical coupling conditions, allowing further functionalization in multi-step syntheses. It is particularly useful in drug discovery and development for building complex aromatic frameworks with high selectivity and yield.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿410.00
inventory 5g
10-20 days ฿1,980.00
inventory 25g
10-20 days ฿9,150.00

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tert-Butyl 3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzoate
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Widely used in Suzuki-Miyaura cross-coupling reactions, this compound serves as a key boronic ester reagent for forming carbon-carbon bonds in organic synthesis. Its stability and reactivity make it valuable for constructing biaryl and aryl systems found in pharmaceuticals, agrochemicals, and advanced materials. The tert-butyl ester group remains intact under typical coupling conditions, allowing further functionalization in multi-step syntheses. It is particularly useful in drug discovery and developmen

Widely used in Suzuki-Miyaura cross-coupling reactions, this compound serves as a key boronic ester reagent for forming carbon-carbon bonds in organic synthesis. Its stability and reactivity make it valuable for constructing biaryl and aryl systems found in pharmaceuticals, agrochemicals, and advanced materials. The tert-butyl ester group remains intact under typical coupling conditions, allowing further functionalization in multi-step syntheses. It is particularly useful in drug discovery and development for building complex aromatic frameworks with high selectivity and yield.

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