(1-(Thiophen-3-yl)-1H-pyrazol-4-yl)boronic acid

95%

Reagent Code: #88978
fingerprint
CAS Number 1974329-41-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 194.02 g/mol
Formula C₇H₇BN₂O₂S
badge Registry Numbers
MDL Number MFCD21099655
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 building block for the formation of carbon-carbon bonds, enabling the creation of complex organic molecules. Its boronic acid functional group allows it to react with various aryl or vinyl halides in the presence of a palladium catalyst, making it valuable in the development of pharmaceuticals, agrochemicals, and advanced materials. Additionally, its thiophene and pyrazole moieties contribute to its potential use in designing molecules with specific electronic or biological properties, such as in drug discovery for targeting specific enzymes or receptors.

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