4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)benzonitrile

98%

Reagent Code: #90742
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CAS Number 171364-82-2

science Other reagents with same CAS 171364-82-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 229.0800 g/mol
Formula C₁₃H₁₆BNO₂
badge Registry Numbers
MDL Number MFCD03093897
inventory_2 Storage & Handling
Storage room temperature

description Product Description

Used as a key intermediate in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, which are widely employed in the production of pharmaceuticals, agrochemicals, and advanced materials. Its boronate ester group facilitates the formation of carbon-carbon bonds, enabling the construction of complex organic molecules. Additionally, it serves as a precursor in the development of liquid crystals and organic light-emitting diodes (OLEDs), contributing to advancements in display technologies. Its nitrile group also allows for further functionalization, making it versatile in the synthesis of various bioactive compounds and polymers.

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Test Parameter Specification
Purity (GC) 97.5-100%
Melting point 94-99
Appearance White to Tan to Very Dark Orange Powder, Crystals or Crystalline Powder

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿380.00
inventory 5g
10-20 days ฿1,560.00
inventory 25g
10-20 days ฿6,800.00
inventory 100g
10-20 days ฿19,200.00

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4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)benzonitrile
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Used as a key intermediate in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, which are widely employed in the production of pharmaceuticals, agrochemicals, and advanced materials. Its boronate ester group facilitates the formation of carbon-carbon bonds, enabling the construction of complex organic molecules. Additionally, it serves as a precursor in the development of liquid crystals and organic light-emitting diodes (OLEDs), contributing to advancements in display technolog

Used as a key intermediate in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, which are widely employed in the production of pharmaceuticals, agrochemicals, and advanced materials. Its boronate ester group facilitates the formation of carbon-carbon bonds, enabling the construction of complex organic molecules. Additionally, it serves as a precursor in the development of liquid crystals and organic light-emitting diodes (OLEDs), contributing to advancements in display technologies. Its nitrile group also allows for further functionalization, making it versatile in the synthesis of various bioactive compounds and polymers.

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