3-Methoxy-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenol

97%

Reagent Code: #118153
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CAS Number 507462-88-6

science Other reagents with same CAS 507462-88-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 250.10 g/mol
Formula C₁₃H₁₉BO₄
badge Registry Numbers
MDL Number MFCD16994337
inventory_2 Storage & Handling
Storage 2-8°C, store under inert gas

description Product Description

Used primarily in organic synthesis, this compound serves as a key intermediate in the preparation of various pharmaceuticals and bioactive molecules. Its boronate ester group enables it to participate in Suzuki-Miyaura cross-coupling reactions, a widely utilized method for forming carbon-carbon bonds. This makes it valuable in the development of complex organic compounds, including drug candidates and advanced materials. Additionally, its phenolic moiety allows for further functionalization, enhancing its versatility in chemical transformations. It is particularly useful in the synthesis of polyphenols and other aromatic compounds with potential applications in medicinal chemistry and material science.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿10,410.00
inventory 5g
10-20 days ฿49,990.00
inventory 100mg
10-20 days ฿2,180.00
inventory 250mg
10-20 days ฿3,470.00

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3-Methoxy-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenol
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Used primarily in organic synthesis, this compound serves as a key intermediate in the preparation of various pharmaceuticals and bioactive molecules. Its boronate ester group enables it to participate in Suzuki-Miyaura cross-coupling reactions, a widely utilized method for forming carbon-carbon bonds. This makes it valuable in the development of complex organic compounds, including drug candidates and advanced materials. Additionally, its phenolic moiety allows for further functionalization, enhancing i

Used primarily in organic synthesis, this compound serves as a key intermediate in the preparation of various pharmaceuticals and bioactive molecules. Its boronate ester group enables it to participate in Suzuki-Miyaura cross-coupling reactions, a widely utilized method for forming carbon-carbon bonds. This makes it valuable in the development of complex organic compounds, including drug candidates and advanced materials. Additionally, its phenolic moiety allows for further functionalization, enhancing its versatility in chemical transformations. It is particularly useful in the synthesis of polyphenols and other aromatic compounds with potential applications in medicinal chemistry and material science.

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