2-Methyl-5-(pyrrolidino)thiophene-3-boronic acid pinacol ester

95%

Reagent Code: #89756
fingerprint
CAS Number 2223031-27-2

science Other reagents with same CAS 2223031-27-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 311.24784 g/mol
Formula C₁₅H₂₆BNO₃S
inventory_2 Storage & Handling
Storage -20°C, sealed, dry

description Product Description

Used primarily in organic synthesis, this compound serves as a key intermediate in cross-coupling reactions, such as Suzuki-Miyaura coupling. It facilitates the formation of carbon-carbon bonds, enabling the construction of complex thiophene derivatives. These derivatives are valuable in the development of pharmaceuticals, agrochemicals, and organic electronic materials, including semiconductors and light-emitting diodes (LEDs). Its boronic ester group enhances stability and reactivity, making it suitable for use in mild reaction conditions. Additionally, it plays a role in the synthesis of bioactive molecules and advanced materials for optoelectronic applications.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 5mg
10-20 days ฿10,782.00
inventory 25mg
10-20 days ฿31,734.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
2-Methyl-5-(pyrrolidino)thiophene-3-boronic acid pinacol ester
No image available

Used primarily in organic synthesis, this compound serves as a key intermediate in cross-coupling reactions, such as Suzuki-Miyaura coupling. It facilitates the formation of carbon-carbon bonds, enabling the construction of complex thiophene derivatives. These derivatives are valuable in the development of pharmaceuticals, agrochemicals, and organic electronic materials, including semiconductors and light-emitting diodes (LEDs). Its boronic ester group enhances stability and reactivity, making it suitabl

Used primarily in organic synthesis, this compound serves as a key intermediate in cross-coupling reactions, such as Suzuki-Miyaura coupling. It facilitates the formation of carbon-carbon bonds, enabling the construction of complex thiophene derivatives. These derivatives are valuable in the development of pharmaceuticals, agrochemicals, and organic electronic materials, including semiconductors and light-emitting diodes (LEDs). Its boronic ester group enhances stability and reactivity, making it suitable for use in mild reaction conditions. Additionally, it plays a role in the synthesis of bioactive molecules and advanced materials for optoelectronic applications.

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...