5-(3-Fluorophenyl)thiazole-4-boronic acid pinacol ester

95%

Reagent Code: #90776
fingerprint
CAS Number 2223054-37-1

science Other reagents with same CAS 2223054-37-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 323.1906632 g/mol
Formula C₁₅H₁₉BFNO₃S
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 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 biaryl or styryl structures. This makes it valuable in the synthesis of drug candidates, agrochemicals, and advanced materials. Additionally, its fluorophenyl moiety can enhance the biological activity or metabolic stability of the resulting compounds, making it a useful building block in medicinal chemistry.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 5mg
10-20 days ฿8,280.00
inventory 25mg
10-20 days ฿24,300.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
5-(3-Fluorophenyl)thiazole-4-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 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 biaryl or styryl structures. This makes it valuable in the synthesis of drug candidates, agrochemicals, and advanced materials. Additionally, its

This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura coupling. 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 biaryl or styryl structures. This makes it valuable in the synthesis of drug candidates, agrochemicals, and advanced materials. Additionally, its fluorophenyl moiety can enhance the biological activity or metabolic stability of the resulting compounds, making it a useful building block in medicinal 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...