3-Methoxythiophene-2-boronic acid pinacol ester

98%

Reagent Code: #208561
fingerprint
CAS Number 1310384-98-5

science Other reagents with same CAS 1310384-98-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 240.1300 g/mol
Formula C₁₁H₁₇BO₃S
badge Registry Numbers
MDL Number MFCD09837621
thermostat Physical Properties
Melting Point 124-128℃
Boiling Point 333.1±27.0℃(Predicted)
inventory_2 Storage & Handling
Density 1.10±0.1g/ml(Predicted)
Storage 2-8℃, dry, sealed

description Product Description

Used in Suzuki-Miyaura cross-coupling reactions to synthesize conjugated organic materials, especially in the development of organic semiconductors and conductive polymers. Its boronic ester group enables efficient carbon-carbon bond formation under mild conditions, making it valuable in pharmaceutical and agrochemical research for building complex heterocyclic systems. Commonly employed in the preparation of thiophene-based functional molecules for optoelectronic devices such as OLEDs and organic solar cells.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿3,040.00
inventory 5g
10-20 days ฿8,440.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
3-Methoxythiophene-2-boronic acid pinacol ester
No image available

Used in Suzuki-Miyaura cross-coupling reactions to synthesize conjugated organic materials, especially in the development of organic semiconductors and conductive polymers. Its boronic ester group enables efficient carbon-carbon bond formation under mild conditions, making it valuable in pharmaceutical and agrochemical research for building complex heterocyclic systems. Commonly employed in the preparation of thiophene-based functional molecules for optoelectronic devices such as OLEDs and organic solar

Used in Suzuki-Miyaura cross-coupling reactions to synthesize conjugated organic materials, especially in the development of organic semiconductors and conductive polymers. Its boronic ester group enables efficient carbon-carbon bond formation under mild conditions, making it valuable in pharmaceutical and agrochemical research for building complex heterocyclic systems. Commonly employed in the preparation of thiophene-based functional molecules for optoelectronic devices such as OLEDs and organic solar cells.

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...