1-Methyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-benzo[d][1,2,3]triazole

98%

Reagent Code: #40151
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CAS Number 1396753-41-5

science Other reagents with same CAS 1396753-41-5

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Weight 259.1119 g/mol
Formula C₁₃H₁₈BN₃O₂
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

This chemical is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction, where it serves as a boron-containing reagent. Its structure, featuring a benzo[d][1,2,3]triazole moiety, makes it a valuable intermediate in the preparation of complex organic molecules, including pharmaceuticals, agrochemicals, and advanced materials. The presence of the tetramethyl dioxaborolane group enhances its stability and reactivity, facilitating efficient transformations under mild conditions. Additionally, it is employed in the development of fluorescent dyes and sensors due to its ability to participate in conjugation and electron transfer processes.

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inventory 25mg
10-20 days ฿6,624.00

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1-Methyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-benzo[d][1,2,3]triazole
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This chemical is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction, where it serves as a boron-containing reagent. Its structure, featuring a benzo[d][1,2,3]triazole moiety, makes it a valuable intermediate in the preparation of complex organic molecules, including pharmaceuticals, agrochemicals, and advanced materials. The presence of the tetramethyl dioxaborolane group enhances its stability and reactivity, facilitating efficient trans

This chemical is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction, where it serves as a boron-containing reagent. Its structure, featuring a benzo[d][1,2,3]triazole moiety, makes it a valuable intermediate in the preparation of complex organic molecules, including pharmaceuticals, agrochemicals, and advanced materials. The presence of the tetramethyl dioxaborolane group enhances its stability and reactivity, facilitating efficient transformations under mild conditions. Additionally, it is employed in the development of fluorescent dyes and sensors due to its ability to participate in conjugation and electron transfer processes.

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