2-Chloro-6-methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenol

97%

Reagent Code: #116527
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CAS Number 1294518-25-4

science Other reagents with same CAS 1294518-25-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 268.54 g/mol
Formula C₁₃H₁₈BClO₃
badge Registry Numbers
MDL Number MFCD22414580
inventory_2 Storage & Handling
Storage 2-8°C, store under inert gas

description Product Description

This chemical is primarily utilized in organic synthesis as a key intermediate in the preparation of complex molecules. It is particularly valuable in cross-coupling reactions, such as the Suzuki-Miyaura reaction, where it acts as a boron-containing reagent to form carbon-carbon bonds efficiently. This makes it a crucial component in the development of pharmaceuticals, agrochemicals, and advanced materials. Its boronate ester group provides stability and reactivity, enabling precise control in the synthesis of target compounds. Additionally, it is employed in the production of functionalized aromatic compounds, which are essential in the design of drugs and organic electronic materials.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿6,912.00
inventory 100mg
10-20 days ฿3,807.00
inventory 1g
10-20 days ฿17,289.00

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2-Chloro-6-methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenol
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This chemical is primarily utilized in organic synthesis as a key intermediate in the preparation of complex molecules. It is particularly valuable in cross-coupling reactions, such as the Suzuki-Miyaura reaction, where it acts as a boron-containing reagent to form carbon-carbon bonds efficiently. This makes it a crucial component in the development of pharmaceuticals, agrochemicals, and advanced materials. Its boronate ester group provides stability and reactivity, enabling precise control in the synthesis of target compounds. Additionally, it is employed in the production of functionalized aromatic compounds, which are essential in the design of drugs and organic electronic materials.
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