5-(iso-Propyl)thiazole-4-boronic acid pinacol ester

95%

Reagent Code: #90832
fingerprint
CAS Number 2223029-15-8

science Other reagents with same CAS 2223029-15-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 271.18398 g/mol
Formula C₁₂H₂₂BNO₃S
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. Its boronic ester group makes it a valuable intermediate for constructing complex molecules, especially in the pharmaceutical and agrochemical industries. It is often employed to introduce the thiazole moiety into target compounds, which is a key structural feature in many biologically active molecules. Additionally, its stability and reactivity under mild conditions make it a preferred choice for synthesizing heterocyclic compounds used in drug discovery and development.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 25mg
10-20 days ฿96,000.00
inventory 100mg
10-20 days ฿285,000.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
5-(iso-Propyl)thiazole-4-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. Its boronic ester group makes it a valuable intermediate for constructing complex molecules, especially in the pharmaceutical and agrochemical industries. It is often employed to introduce the thiazole moiety into target compounds, which is a key structural feature in many biologically active molecules. Additionally, its stability and reactivity under mild conditions mak

This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. Its boronic ester group makes it a valuable intermediate for constructing complex molecules, especially in the pharmaceutical and agrochemical industries. It is often employed to introduce the thiazole moiety into target compounds, which is a key structural feature in many biologically active molecules. Additionally, its stability and reactivity under mild conditions make it a preferred choice for synthesizing heterocyclic compounds used in drug discovery and development.

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...