1,2-Bis(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)ethyne

98%(GC)

Reagent Code: #149380
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CAS Number 1010840-17-1

science Other reagents with same CAS 1010840-17-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 277.96 g/mol
Formula C₁₄H₂₄B₂O₄
badge Registry Numbers
MDL Number MFCD22666429
thermostat Physical Properties
Melting Point 269 °C
Boiling Point 272 °C
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used primarily in organic synthesis as a key building block for cross-coupling reactions, especially in the Suzuki-Miyaura coupling. This compound enables the formation of conjugated alkynes, which are important in the development of organic electronic materials such as semiconductors, light-emitting diodes (OLEDs), and molecular wires. Its boronate ester groups provide high stability and reactivity, making it ideal for iterative synthesis in constructing extended π-conjugated systems. It is also employed in the preparation of functional polymers and metal-organic frameworks (MOFs) where precise molecular architecture is required.

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Test Parameter Specification
Appearance White to Off-white Powder or Crystals
Purity 97.5-100%
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿2,980.00
inventory 250mg
10-20 days ฿5,960.00

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1,2-Bis(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)ethyne
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Used primarily in organic synthesis as a key building block for cross-coupling reactions, especially in the Suzuki-Miyaura coupling. This compound enables the formation of conjugated alkynes, which are important in the development of organic electronic materials such as semiconductors, light-emitting diodes (OLEDs), and molecular wires. Its boronate ester groups provide high stability and reactivity, making it ideal for iterative synthesis in constructing extended π-conjugated systems. It is also employe

Used primarily in organic synthesis as a key building block for cross-coupling reactions, especially in the Suzuki-Miyaura coupling. This compound enables the formation of conjugated alkynes, which are important in the development of organic electronic materials such as semiconductors, light-emitting diodes (OLEDs), and molecular wires. Its boronate ester groups provide high stability and reactivity, making it ideal for iterative synthesis in constructing extended π-conjugated systems. It is also employed in the preparation of functional polymers and metal-organic frameworks (MOFs) where precise molecular architecture is required.

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