2-(Benzo[b]thiophen-5-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

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Reagent Code: #115576
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CAS Number 501945-71-7

science Other reagents with same CAS 501945-71-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 260.16 g/mol
Formula C₁₄H₁₇BO₂S
badge Registry Numbers
MDL Number MFCD05664405
thermostat Physical Properties
Boiling Point 377.7°C at 760 mmHg
inventory_2 Storage & Handling
Density 1.13g/cm3
Storage 2-8°C, protected from light, stored in an inert gas

description Product Description

This chemical is primarily used as a key intermediate in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura coupling. It is valuable in the development of pharmaceuticals, agrochemicals, and advanced materials. Its boronate ester group enables efficient formation of carbon-carbon bonds, making it essential for constructing complex organic molecules. Additionally, it is utilized in the synthesis of organic electronic materials, including polymers and small molecules for OLEDs and organic photovoltaics, due to its ability to introduce benzo[b]thiophene moieties, which are known for their optoelectronic properties.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,269.00
inventory 250mg
10-20 days ฿2,088.00
inventory 1g
10-20 days ฿5,607.00
inventory 5g
10-20 days ฿25,308.00

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2-(Benzo[b]thiophen-5-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
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This chemical is primarily used as a key intermediate in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura coupling. It is valuable in the development of pharmaceuticals, agrochemicals, and advanced materials. Its boronate ester group enables efficient formation of carbon-carbon bonds, making it essential for constructing complex organic molecules. Additionally, it is utilized in the synthesis of organic electronic materials, including polymers and small molecules for OLE

This chemical is primarily used as a key intermediate in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura coupling. It is valuable in the development of pharmaceuticals, agrochemicals, and advanced materials. Its boronate ester group enables efficient formation of carbon-carbon bonds, making it essential for constructing complex organic molecules. Additionally, it is utilized in the synthesis of organic electronic materials, including polymers and small molecules for OLEDs and organic photovoltaics, due to its ability to introduce benzo[b]thiophene moieties, which are known for their optoelectronic properties.

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