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

95%

Reagent Code: #90393
fingerprint
CAS Number 2223050-58-4

science Other reagents with same CAS 2223050-58-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 306.18826 g/mol
Formula C₁₄H₁₉BN₂O₃S
inventory_2 Storage & Handling
Storage -20°C, sealed, dry

description Product Description

Used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, to create complex molecules for pharmaceuticals and materials science. Acts as a key intermediate in the development of bioactive compounds, including potential drugs targeting various diseases. Its boronic ester group facilitates efficient coupling with aryl halides, enabling the construction of carbon-carbon bonds. Also employed in the synthesis of advanced organic materials, such as conjugated polymers for electronic devices. Its pyridyl and thiazole moieties contribute to its utility in designing molecules with specific biological or electronic properties.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 5mg
10-20 days ฿10,080.00
inventory 25mg
10-20 days ฿29,304.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
4-(3-Pyridyl)thiazole-5-boronic acid pinacol ester
No image available

Used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, to create complex molecules for pharmaceuticals and materials science. Acts as a key intermediate in the development of bioactive compounds, including potential drugs targeting various diseases. Its boronic ester group facilitates efficient coupling with aryl halides, enabling the construction of carbon-carbon bonds. Also employed in the synthesis of advanced organic materials, such as conjugated polymers for electronic d

Used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, to create complex molecules for pharmaceuticals and materials science. Acts as a key intermediate in the development of bioactive compounds, including potential drugs targeting various diseases. Its boronic ester group facilitates efficient coupling with aryl halides, enabling the construction of carbon-carbon bonds. Also employed in the synthesis of advanced organic materials, such as conjugated polymers for electronic devices. Its pyridyl and thiazole moieties contribute to its utility in designing molecules with specific biological or electronic properties.

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...