5-(4-Pyridyl)thiophene-2-boronic acid pinacol ester

95%

Reagent Code: #90810
fingerprint
CAS Number 1402240-70-3

science Other reagents with same CAS 1402240-70-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 305.2002 g/mol
Formula C₁₅H₂₀BNO₃S
inventory_2 Storage & Handling
Storage -20°C, sealed, dry

description Product Description

This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. It serves as a key intermediate for constructing complex organic molecules, especially in the development of pharmaceuticals and agrochemicals. Its boronic ester group enables efficient coupling with aryl halides, facilitating the formation of carbon-carbon bonds. Additionally, it is employed in the synthesis of conjugated polymers and materials for organic electronics, including OLEDs and organic photovoltaics, due to its ability to introduce functional pyridyl and thiophene moieties into the polymer backbone. Its applications also extend to the preparation of ligands for catalysis and metal-organic frameworks (MOFs) for gas storage and separation.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 5mg
10-20 days ฿8,982.00
inventory 25mg
10-20 days ฿19,800.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
5-(4-Pyridyl)thiophene-2-boronic acid pinacol ester
No image available

This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. It serves as a key intermediate for constructing complex organic molecules, especially in the development of pharmaceuticals and agrochemicals. Its boronic ester group enables efficient coupling with aryl halides, facilitating the formation of carbon-carbon bonds. Additionally, it is employed in the synthesis of conjugated polymers and materials for organic electronics,

This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. It serves as a key intermediate for constructing complex organic molecules, especially in the development of pharmaceuticals and agrochemicals. Its boronic ester group enables efficient coupling with aryl halides, facilitating the formation of carbon-carbon bonds. Additionally, it is employed in the synthesis of conjugated polymers and materials for organic electronics, including OLEDs and organic photovoltaics, due to its ability to introduce functional pyridyl and thiophene moieties into the polymer backbone. Its applications also extend to the preparation of ligands for catalysis and metal-organic frameworks (MOFs) for gas storage and separation.

Mechanism -
Appearance -
Longevity -
Strength -
Storage -
Shelf Life -
Allergen(s) -
Dosage (Range) -
Dosage (Per Day) -
Mix Method -
Heat Resistance -
Stable in pH range -
Solubility -
Product Types -
INCI -

Purchase History for

Loading purchase history...