2-(4-Isobutylphenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

98%

Reagent Code: #115723
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CAS Number 1033753-01-3

science Other reagents with same CAS 1033753-01-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 260.18 g/mol
Formula C₁₆H₂₅BO₂
badge Registry Numbers
MDL Number MFCD05663842
inventory_2 Storage & Handling
Storage Room temperature, sealed, dry

description Product Description

This compound is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key intermediate for constructing complex organic molecules, especially in the pharmaceutical and agrochemical industries. Its boronate ester group facilitates the formation of carbon-carbon bonds, enabling the synthesis of biaryl compounds, which are essential in developing drugs and functional materials. Additionally, it is employed in the preparation of advanced materials, such as liquid crystals and organic semiconductors, due to its ability to introduce aromatic structures into molecular frameworks. Its stability and reactivity make it a valuable tool in modern synthetic chemistry.

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Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿8,775.00
inventory 250mg
10-20 days ฿1,116.00
inventory 1g
10-20 days ฿2,925.00

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2-(4-Isobutylphenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
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This compound is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key intermediate for constructing complex organic molecules, especially in the pharmaceutical and agrochemical industries. Its boronate ester group facilitates the formation of carbon-carbon bonds, enabling the synthesis of biaryl compounds, which are essential in developing drugs and functional materials. Additionally, it is employed in the preparation of advanced materials,

This compound is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key intermediate for constructing complex organic molecules, especially in the pharmaceutical and agrochemical industries. Its boronate ester group facilitates the formation of carbon-carbon bonds, enabling the synthesis of biaryl compounds, which are essential in developing drugs and functional materials. Additionally, it is employed in the preparation of advanced materials, such as liquid crystals and organic semiconductors, due to its ability to introduce aromatic structures into molecular frameworks. Its stability and reactivity make it a valuable tool in modern synthetic chemistry.

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