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

≥95%

Reagent Code: #119422
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CAS Number 882670-69-1

science Other reagents with same CAS 882670-69-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 233.11 g/mol
Formula C₁₃H₂₀BNO₂
badge Registry Numbers
MDL Number MFCD05663859
thermostat Physical Properties
Boiling Point 366.2°C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, protected from light, stored in an inert gas

description Product Description

Used in organic synthesis as a key intermediate for the preparation of pharmaceuticals and agrochemicals. It is particularly valuable in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds, which is essential for creating complex organic molecules. The compound’s boronate ester group enhances its reactivity and selectivity in these reactions. Additionally, it serves as a building block in the development of advanced materials, such as organic semiconductors and polymers, due to its ability to introduce functional groups into aromatic systems. Its applications also extend to the field of medicinal chemistry, where it is utilized in the synthesis of drug candidates targeting various diseases.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿594.00
inventory 25g
10-20 days ฿13,320.00
inventory 250mg
10-20 days ฿315.00
inventory 5g
10-20 days ฿2,880.00
inventory 10g
10-20 days ฿5,562.00

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4-Methyl-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)aniline
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Used in organic synthesis as a key intermediate for the preparation of pharmaceuticals and agrochemicals. It is particularly valuable in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds, which is essential for creating complex organic molecules. The compound’s boronate ester group enhances its reactivity and selectivity in these reactions. Additionally, it serves as a building block in the development of advanced materials, such as organic semiconductors and polymers, due to its ability to introduce functional groups into aromatic systems. Its applications also extend to the field of medicinal chemistry, where it is utilized in the synthesis of drug candidates targeting various diseases.
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