4-(2-Methylpiperidin-1-yl)thiophene-2-boronic acid pinacol ester

95%

Reagent Code: #90348
fingerprint
CAS Number 2223009-25-2

science Other reagents with same CAS 2223009-25-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 325.27442 g/mol
Formula C₁₆H₂₈BNO₃S
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 Suzuki-Miyaura coupling. It serves as a crucial intermediate for constructing complex molecules, especially in the pharmaceutical and agrochemical industries. Its boronic ester group enables efficient coupling with aryl or vinyl halides, facilitating the formation of carbon-carbon bonds. This makes it valuable in the development of active pharmaceutical ingredients (APIs) and other fine chemicals. Additionally, it finds use in materials science for synthesizing organic electronic materials, including polymers and small molecules for optoelectronic applications. Its stability and reactivity under mild conditions make it a preferred choice in modern synthetic chemistry.

shopping_cart Available Sizes & Pricing

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

Cart

No products

Subtotal: 0.00
Total 0.00 THB
4-(2-Methylpiperidin-1-yl)thiophene-2-boronic acid pinacol ester
No image available

This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura coupling. It serves as a crucial intermediate for constructing complex molecules, especially in the pharmaceutical and agrochemical industries. Its boronic ester group enables efficient coupling with aryl or vinyl halides, facilitating the formation of carbon-carbon bonds. This makes it valuable in the development of active pharmaceutical ingredients (APIs) and other fine chemicals. A

This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura coupling. It serves as a crucial intermediate for constructing complex molecules, especially in the pharmaceutical and agrochemical industries. Its boronic ester group enables efficient coupling with aryl or vinyl halides, facilitating the formation of carbon-carbon bonds. This makes it valuable in the development of active pharmaceutical ingredients (APIs) and other fine chemicals. Additionally, it finds use in materials science for synthesizing organic electronic materials, including polymers and small molecules for optoelectronic applications. Its stability and reactivity under mild conditions make it a preferred choice in modern synthetic chemistry.

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...