2-(n-Propyl)thiophene-4-boronic acid pinacol ester

95%

Reagent Code: #89667
fingerprint
CAS Number 1595111-51-5

science Other reagents with same CAS 1595111-51-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 270.19592 g/mol
Formula C₁₃H₂₃BO₃S
inventory_2 Storage & Handling
Storage -20°C, sealed, dry

description Product Description

2-(n-Propyl)thiophene-4-boronic acid pinacol ester is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This compound serves as a key intermediate in the preparation of complex organic molecules, especially in the pharmaceutical and agrochemical industries. Its boronic ester group facilitates the formation of carbon-carbon bonds, making it valuable for constructing biaryl compounds and heterocycles. Additionally, it is employed in the development of organic electronic materials, such as polymers and small molecules for use in OLEDs and organic photovoltaics, due to its thiophene backbone, which enhances electronic properties. Its stability and reactivity under mild conditions make it a preferred choice in various catalytic processes.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 25mg
10-20 days ฿44,800.00
inventory 100mg
10-20 days ฿134,400.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
2-(n-Propyl)thiophene-4-boronic acid pinacol ester
No image available

2-(n-Propyl)thiophene-4-boronic acid pinacol ester is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This compound serves as a key intermediate in the preparation of complex organic molecules, especially in the pharmaceutical and agrochemical industries. Its boronic ester group facilitates the formation of carbon-carbon bonds, making it valuable for constructing biaryl compounds and heterocycles. Additionally, it is employed in the development of organic electr

2-(n-Propyl)thiophene-4-boronic acid pinacol ester is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This compound serves as a key intermediate in the preparation of complex organic molecules, especially in the pharmaceutical and agrochemical industries. Its boronic ester group facilitates the formation of carbon-carbon bonds, making it valuable for constructing biaryl compounds and heterocycles. Additionally, it is employed in the development of organic electronic materials, such as polymers and small molecules for use in OLEDs and organic photovoltaics, due to its thiophene backbone, which enhances electronic properties. Its stability and reactivity under mild conditions make it a preferred choice in various catalytic 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...