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

95%

Reagent Code: #115765
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CAS Number 1073339-22-6

science Other reagents with same CAS 1073339-22-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 240.13 g/mol
Formula C₁₁H₁₇BO₃S
badge Registry Numbers
MDL Number MFCD12405477
inventory_2 Storage & Handling
Storage -20°C, dark, inert gas

description Product Description

This chemical is primarily used in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura reactions. It serves as a boronic ester reagent, enabling the formation of carbon-carbon bonds, which is crucial in the development of pharmaceuticals, agrochemicals, and advanced materials. Its methoxy-thiophene moiety makes it valuable in constructing complex molecules, especially in the synthesis of heterocyclic compounds. Additionally, it is employed in the preparation of organic electronic materials, including polymers and small molecules for optoelectronic applications like OLEDs and organic photovoltaics. Its stability and reactivity make it a versatile tool in medicinal chemistry for drug discovery and development.

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

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2-(4-Methoxythiophen-2-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
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This chemical is primarily used in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura reactions. It serves as a boronic ester reagent, enabling the formation of carbon-carbon bonds, which is crucial in the development of pharmaceuticals, agrochemicals, and advanced materials. Its methoxy-thiophene moiety makes it valuable in constructing complex molecules, especially in the synthesis of heterocyclic compounds. Additionally, it is employed in the preparation of organic elec

This chemical is primarily used in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura reactions. It serves as a boronic ester reagent, enabling the formation of carbon-carbon bonds, which is crucial in the development of pharmaceuticals, agrochemicals, and advanced materials. Its methoxy-thiophene moiety makes it valuable in constructing complex molecules, especially in the synthesis of heterocyclic compounds. Additionally, it is employed in the preparation of organic electronic materials, including polymers and small molecules for optoelectronic applications like OLEDs and organic photovoltaics. Its stability and reactivity make it a versatile tool in medicinal chemistry for drug discovery and development.

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