1-pinacolato-2-(1,8)diamo-naphthalenylborane

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Reagent Code: #91242
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CAS Number 1214264-88-6

science Other reagents with same CAS 1214264-88-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 293.96 g/mol
Formula C₁₆H₂₀B₂N₂O₂
badge Registry Numbers
MDL Number MFCD27980593
inventory_2 Storage & Handling
Storage 2-8°C, stored in inert gas

description Product Description

Used as a versatile reagent in organic synthesis, particularly as a coupling partner in Suzuki-Miyaura cross-coupling reactions for the formation of carbon-carbon bonds. It enables the creation of complex organic molecules by transferring the aryl group from boron. Its applications extend to the development of pharmaceuticals, agrochemicals, and advanced materials. The compound is also employed in catalytic systems for selective transformations, enhancing efficiency in synthetic pathways. Its stability and reactivity make it a valuable tool in modern synthetic chemistry.

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Test Parameter Specification
Appearance off-white powder
Purity 96.5-100
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿550.00
inventory 1g
10-20 days ฿2,150.00
inventory 5g
10-20 days ฿9,740.00

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1-pinacolato-2-(1,8)diamo-naphthalenylborane
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Used as a versatile reagent in organic synthesis, particularly as a coupling partner in Suzuki-Miyaura cross-coupling reactions for the formation of carbon-carbon bonds. It enables the creation of complex organic molecules by transferring the aryl group from boron. Its applications extend to the development of pharmaceuticals, agrochemicals, and advanced materials. The compound is also employed in catalytic systems for selective transformations, enhancing efficiency in synthetic pathways. Its stability a

Used as a versatile reagent in organic synthesis, particularly as a coupling partner in Suzuki-Miyaura cross-coupling reactions for the formation of carbon-carbon bonds. It enables the creation of complex organic molecules by transferring the aryl group from boron. Its applications extend to the development of pharmaceuticals, agrochemicals, and advanced materials. The compound is also employed in catalytic systems for selective transformations, enhancing efficiency in synthetic pathways. Its stability and reactivity make it a valuable tool in modern synthetic chemistry.

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