2-(4-(Bromomethyl)-2-chlorophenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

95%

Reagent Code: #90661
label
Alias 4-Bromomethyl-2-chlorophenylboronic acid pinacol ester
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CAS Number 1256360-55-0

science Other reagents with same CAS 1256360-55-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 331.44088 g/mol
Formula C₁₃H₁₇BBrClO₂
badge Registry Numbers
MDL Number MFCD18087736
inventory_2 Storage & Handling
Storage 2~8℃

description Product Description

This chemical 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 the pharmaceutical and agrochemical industries. The bromomethyl and chlorophenyl groups provide additional reactivity, enabling further functionalization or coupling with other compounds. It is often employed in the development of active pharmaceutical ingredients (APIs) and fine chemicals, where precise molecular structures are critical. Additionally, its stability and reactivity make it suitable for use in research and development of new materials or chemical processes.

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Test Parameter Specification
Purity 95-100

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿756.00
inventory 5g
10-20 days ฿2,835.00

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2-(4-(Bromomethyl)-2-chlorophenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
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This chemical 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 the pharmaceutical and agrochemical industries. The bromomethyl and chlorophenyl groups provide additional reactivity, enabling further functionalization or coupling with other compounds. It is often employed in the development of active pharmaceutical ingr

This chemical 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 the pharmaceutical and agrochemical industries. The bromomethyl and chlorophenyl groups provide additional reactivity, enabling further functionalization or coupling with other compounds. It is often employed in the development of active pharmaceutical ingredients (APIs) and fine chemicals, where precise molecular structures are critical. Additionally, its stability and reactivity make it suitable for use in research and development of new materials or chemical processes.

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