5-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-benzo[d]imidazol-2(3H)-one

95%

Reagent Code: #241661
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CAS Number 710348-69-9

science Other reagents with same CAS 710348-69-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 260.10 g/mol
Formula C₁₃H₁₇BN₂O₃
badge Registry Numbers
MDL Number MFCD09260491
thermostat Physical Properties
Boiling Point 304.6°C at 760 mmHg
inventory_2 Storage & Handling
Density 1.21g/cm3
Storage 2-8°C, stored in inert gas

description Product Description

Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions for the synthesis of biologically active compounds, particularly in pharmaceutical and agrochemical research. Its boronate ester group enables efficient carbon-carbon bond formation under mild conditions, making it valuable in the development of novel heterocyclic systems. Commonly employed in medicinal chemistry for constructing benzimidazole-based scaffolds, which are found in drugs with antiviral, anticancer, and anti-inflammatory properties. Also utilized in materials science for designing organic semiconductors and fluorescent probes due to the electron-rich nature of the benzimidazole core.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,010.00
inventory 250mg
10-20 days ฿2,120.00
inventory 1g
10-20 days ฿7,280.00
inventory 5g
10-20 days ฿33,250.00

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5-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-benzo[d]imidazol-2(3H)-one
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Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions for the synthesis of biologically active compounds, particularly in pharmaceutical and agrochemical research. Its boronate ester group enables efficient carbon-carbon bond formation under mild conditions, making it valuable in the development of novel heterocyclic systems. Commonly employed in medicinal chemistry for constructing benzimidazole-based scaffolds, which are found in drugs with antiviral, anticancer, and anti-inflammatory prop
Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions for the synthesis of biologically active compounds, particularly in pharmaceutical and agrochemical research. Its boronate ester group enables efficient carbon-carbon bond formation under mild conditions, making it valuable in the development of novel heterocyclic systems. Commonly employed in medicinal chemistry for constructing benzimidazole-based scaffolds, which are found in drugs with antiviral, anticancer, and anti-inflammatory properties. Also utilized in materials science for designing organic semiconductors and fluorescent probes due to the electron-rich nature of the benzimidazole core.
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