4,4,5,5-Tetramethyl-2-(4-(methylsulfinyl)phenyl)-1,3,2-dioxaborolane

95%

Reagent Code: #118377
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CAS Number 1016641-70-5

science Other reagents with same CAS 1016641-70-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 266.16 g/mol
Formula C₁₃H₁₉BO₃S
badge Registry Numbers
MDL Number MFCD16660301
thermostat Physical Properties
Boiling Point 399.2±25.0 °C at 760 mmHg
inventory_2 Storage & Handling
Storage room temperature, inert gas

description Product Description

This chemical is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key boron reagent, enabling the formation of carbon-carbon bonds between aryl or vinyl boronic esters and aryl or vinyl halides. This makes it valuable in the production of complex organic molecules, including pharmaceuticals, agrochemicals, and advanced materials. Its stability and reactivity under mild conditions make it a preferred choice in medicinal chemistry for developing drug candidates. Additionally, it is employed in the synthesis of conjugated polymers and organic electronic materials, contributing to advancements in optoelectronics and nanotechnology.

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

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4,4,5,5-Tetramethyl-2-(4-(methylsulfinyl)phenyl)-1,3,2-dioxaborolane
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This chemical is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key boron reagent, enabling the formation of carbon-carbon bonds between aryl or vinyl boronic esters and aryl or vinyl halides. This makes it valuable in the production of complex organic molecules, including pharmaceuticals, agrochemicals, and advanced materials. Its stability and reactivity under mild conditions make it a preferred choice in medicinal chemistry for developi

This chemical is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key boron reagent, enabling the formation of carbon-carbon bonds between aryl or vinyl boronic esters and aryl or vinyl halides. This makes it valuable in the production of complex organic molecules, including pharmaceuticals, agrochemicals, and advanced materials. Its stability and reactivity under mild conditions make it a preferred choice in medicinal chemistry for developing drug candidates. Additionally, it is employed in the synthesis of conjugated polymers and organic electronic materials, contributing to advancements in optoelectronics and nanotechnology.

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