2-(3-Buten-1-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

≥97%, containing stabilizer phenothiazine

Reagent Code: #89622
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CAS Number 331958-92-0

science Other reagents with same CAS 331958-92-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 182.07 g/mol
Formula C₁₀H₁₉BO₂
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MDL Number MFCD11858602
inventory_2 Storage & Handling
Storage room temperature, dry

description Product Description

This chemical is primarily used in organic synthesis as a versatile building block for the introduction of boron-containing groups into molecules. It is particularly valuable in Suzuki-Miyaura cross-coupling reactions, a widely employed method for forming carbon-carbon bonds in the synthesis of pharmaceuticals, agrochemicals, and advanced materials. Its stability and reactivity make it suitable for creating complex organic compounds, including those used in drug discovery and development. Additionally, it serves as a precursor in the preparation of boron-based polymers and materials with applications in electronics and optoelectronics. Its role in facilitating efficient and selective chemical transformations underscores its importance in modern synthetic chemistry.

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Size Availability Unit Price Quantity
inventory 200mg
10-20 days ฿1,161.00
inventory 1g
10-20 days ฿4,455.00

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2-(3-Buten-1-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
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This chemical is primarily used in organic synthesis as a versatile building block for the introduction of boron-containing groups into molecules. It is particularly valuable in Suzuki-Miyaura cross-coupling reactions, a widely employed method for forming carbon-carbon bonds in the synthesis of pharmaceuticals, agrochemicals, and advanced materials. Its stability and reactivity make it suitable for creating complex organic compounds, including those used in drug discovery and development. Additionally, it serves as a precursor in the preparation of boron-based polymers and materials with applications in electronics and optoelectronics. Its role in facilitating efficient and selective chemical transformations underscores its importance in modern synthetic chemistry.
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