5-(N-Methylpiperazin-1-yl)furan-2-boronic acid pinacol ester

95%

Reagent Code: #90837
fingerprint
CAS Number 2223051-15-6

science Other reagents with same CAS 2223051-15-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 310.19688 g/mol
Formula C₁₅H₂₇BN₂O₄
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 molecules, especially in pharmaceutical research and development. Its boronic ester group enables efficient coupling with aryl or vinyl halides, facilitating the creation of carbon-carbon bonds. This property makes it valuable in the synthesis of biologically active compounds, including potential drug candidates. Additionally, it is employed in the development of materials science applications, where precise molecular assembly is required. Its stability and reactivity profile make it a versatile reagent in medicinal chemistry and industrial processes.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿46,602.00
inventory 25mg
10-20 days ฿15,552.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
5-(N-Methylpiperazin-1-yl)furan-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 molecules, especially in pharmaceutical research and development. Its boronic ester group enables efficient coupling with aryl or vinyl halides, facilitating the creation of carbon-carbon bonds. This property makes it valuable in the synthesis of biologically active compounds, including potential drug candidates. A

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 molecules, especially in pharmaceutical research and development. Its boronic ester group enables efficient coupling with aryl or vinyl halides, facilitating the creation of carbon-carbon bonds. This property makes it valuable in the synthesis of biologically active compounds, including potential drug candidates. Additionally, it is employed in the development of materials science applications, where precise molecular assembly is required. Its stability and reactivity profile make it a versatile reagent in medicinal chemistry and industrial processes.

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...