Methyl 5-chloro-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzoate

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Reagent Code: #84107
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CAS Number 866625-02-7

science Other reagents with same CAS 866625-02-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 296.55 g/mol
Formula C₁₄H₁₈BClO₄
badge Registry Numbers
MDL Number MFCD16996244
inventory_2 Storage & Handling
Storage Room temperature, dry, sealed

description Product Description

This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. Its boronate ester group makes it a valuable intermediate for constructing complex organic molecules, especially in pharmaceutical and agrochemical research. It is often employed to introduce aromatic rings with specific functional groups into target molecules, aiding in the development of bioactive compounds. Additionally, its stability and reactivity make it suitable for use in materials science, where it can contribute to the synthesis of advanced polymers and organic electronic materials.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,656.00
inventory 250mg
10-20 days ฿2,601.00
inventory 1g
10-20 days ฿6,255.00

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Methyl 5-chloro-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzoate
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This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. Its boronate ester group makes it a valuable intermediate for constructing complex organic molecules, especially in pharmaceutical and agrochemical research. It is often employed to introduce aromatic rings with specific functional groups into target molecules, aiding in the development of bioactive compounds. Additionally, its stability and reactivity make it suitable f

This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. Its boronate ester group makes it a valuable intermediate for constructing complex organic molecules, especially in pharmaceutical and agrochemical research. It is often employed to introduce aromatic rings with specific functional groups into target molecules, aiding in the development of bioactive compounds. Additionally, its stability and reactivity make it suitable for use in materials science, where it can contribute to the synthesis of advanced polymers and organic electronic materials.

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