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

97%

Reagent Code: #116856
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CAS Number 590418-05-6

science Other reagents with same CAS 590418-05-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 233.11 g/mol
Formula C₁₃H₂₀BNO₂
badge Registry Numbers
MDL Number MFCD09033882
thermostat Physical Properties
Boiling Point 359.0±35.0°C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, protected from light, stored in an inert gas

description Product Description

2-Methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)aniline is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This reaction is essential for forming carbon-carbon bonds, making it valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. Its boronate ester group acts as a key intermediate, enabling the introduction of aromatic amines into complex molecules. Additionally, it is employed in the development of organic light-emitting diodes (OLEDs) and other electronic materials due to its ability to modify electronic properties. Its stability and reactivity make it a preferred choice in research and industrial applications for creating diverse organic compounds.

format_list_bulleted Product Specification

Test Parameter Specification
Appearance White to Off-White Solid
Purity (%) 96.5-100
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿3,420.00
inventory 250mg
10-20 days ฿1,764.00
inventory 100mg
10-20 days ฿900.00

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2-Methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)aniline
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2-Methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)aniline is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This reaction is essential for forming carbon-carbon bonds, making it valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. Its boronate ester group acts as a key intermediate, enabling the introduction of aromatic amines into complex molecules. Additionally, it is employed in the development of organic light-emitting

2-Methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)aniline is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This reaction is essential for forming carbon-carbon bonds, making it valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. Its boronate ester group acts as a key intermediate, enabling the introduction of aromatic amines into complex molecules. Additionally, it is employed in the development of organic light-emitting diodes (OLEDs) and other electronic materials due to its ability to modify electronic properties. Its stability and reactivity make it a preferred choice in research and industrial applications for creating diverse organic compounds.

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