tert-butyl3-methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzoate

97%

Reagent Code: #244497
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CAS Number 1073493-92-1

science Other reagents with same CAS 1073493-92-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 318.22 g/mol
Formula C₁₈H₂₇BO₄
badge Registry Numbers
MDL Number MFCD22494127
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used primarily in Suzuki-Miyaura cross-coupling reactions, this compound serves as a key boronic ester reagent in the synthesis of complex organic molecules. Its boron-containing group enables efficient carbon-carbon bond formation under mild conditions, making it valuable in pharmaceutical and agrochemical research. The tert-butyl ester group enhances stability and can be easily deprotected to yield carboxylic acid derivatives, allowing further functionalization. It is especially useful in the preparation of substituted aromatic compounds for drug discovery and materials science.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿6,030.00
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tert-butyl3-methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzoate
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Used primarily in Suzuki-Miyaura cross-coupling reactions, this compound serves as a key boronic ester reagent in the synthesis of complex organic molecules. Its boron-containing group enables efficient carbon-carbon bond formation under mild conditions, making it valuable in pharmaceutical and agrochemical research. The tert-butyl ester group enhances stability and can be easily deprotected to yield carboxylic acid derivatives, allowing further functionalization. It is especially useful in the preparati

Used primarily in Suzuki-Miyaura cross-coupling reactions, this compound serves as a key boronic ester reagent in the synthesis of complex organic molecules. Its boron-containing group enables efficient carbon-carbon bond formation under mild conditions, making it valuable in pharmaceutical and agrochemical research. The tert-butyl ester group enhances stability and can be easily deprotected to yield carboxylic acid derivatives, allowing further functionalization. It is especially useful in the preparation of substituted aromatic compounds for drug discovery and materials science.

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