2-(4-Methoxy-2-nitrophenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

95%

Reagent Code: #115774
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CAS Number 1073353-81-7

science Other reagents with same CAS 1073353-81-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 279.1 g/mol
Formula C₁₃H₁₈BNO₅
badge Registry Numbers
MDL Number MFCD10699701
inventory_2 Storage & Handling
Storage 2-8°C, inert gas

description Product Description

This chemical is primarily used in organic synthesis as a key intermediate in the preparation of various complex molecules. It is particularly valuable in Suzuki-Miyaura cross-coupling reactions, where it acts as a boron-containing reagent to facilitate the formation of carbon-carbon bonds. This makes it essential in the synthesis of pharmaceuticals, agrochemicals, and advanced materials. Additionally, its structure allows for selective functionalization, enabling the creation of tailored compounds for specific applications in drug discovery and development. Its stability and reactivity also make it a preferred choice in research laboratories for constructing diverse organic frameworks.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿3,339.00
inventory 100mg
10-20 days ฿1,971.00
inventory 1g
10-20 days ฿9,000.00

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2-(4-Methoxy-2-nitrophenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
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This chemical is primarily used in organic synthesis as a key intermediate in the preparation of various complex molecules. It is particularly valuable in Suzuki-Miyaura cross-coupling reactions, where it acts as a boron-containing reagent to facilitate the formation of carbon-carbon bonds. This makes it essential in the synthesis of pharmaceuticals, agrochemicals, and advanced materials. Additionally, its structure allows for selective functionalization, enabling the creation of tailored compounds for s

This chemical is primarily used in organic synthesis as a key intermediate in the preparation of various complex molecules. It is particularly valuable in Suzuki-Miyaura cross-coupling reactions, where it acts as a boron-containing reagent to facilitate the formation of carbon-carbon bonds. This makes it essential in the synthesis of pharmaceuticals, agrochemicals, and advanced materials. Additionally, its structure allows for selective functionalization, enabling the creation of tailored compounds for specific applications in drug discovery and development. Its stability and reactivity also make it a preferred choice in research laboratories for constructing diverse organic frameworks.

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