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

98%

Reagent Code: #91058
label
Alias N,N-Dimethyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)aniline 4-(N,N-Dimethylamino)phenylboronic acid pinacol ester
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CAS Number 171364-78-6

science Other reagents with same CAS 171364-78-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 247.15 g/mol
Formula C₁₄H₂₂BNO₂
badge Registry Numbers
MDL Number MFCD05663854
thermostat Physical Properties
Melting Point 122-123°C
inventory_2 Storage & Handling
Storage room temperature

description Product Description

Used in organic synthesis as a key intermediate for the preparation of various pharmaceuticals and agrochemicals. It is particularly valuable in Suzuki-Miyaura cross-coupling reactions, which are widely employed to form carbon-carbon bonds in the production of complex organic molecules. Its boronate ester group facilitates efficient coupling with aryl halides, making it essential in the development of drugs, materials, and fine chemicals. Additionally, it finds application in the synthesis of advanced materials, such as OLEDs and organic semiconductors, due to its ability to introduce aromatic amine functionalities.

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Test Parameter Specification
Melting point 123-127
Purity (GC) 98-100%
Purity (Non-Aqueous Titration) 98-100%
Appearance White to off-white powder or solid or chunks
Infrared Spectrum Conforms to Structure

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿720.00
inventory 5g
10-20 days ฿1,680.00
inventory 25g
10-20 days ฿5,880.00
inventory 100g
10-20 days ฿19,240.00

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N,N-Dimethyl-4-(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 various pharmaceuticals and agrochemicals. It is particularly valuable in Suzuki-Miyaura cross-coupling reactions, which are widely employed to form carbon-carbon bonds in the production of complex organic molecules. Its boronate ester group facilitates efficient coupling with aryl halides, making it essential in the development of drugs, materials, and fine chemicals. Additionally, it finds application in the synthesis of advanced materials, such as OLEDs and organic semiconductors, due to its ability to introduce aromatic amine functionalities.
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