[1,1':3',1''-Terphenyl]-2'-ylboronic acid

95%

Reagent Code: #129691
fingerprint
CAS Number 1065663-52-6

science Other reagents with same CAS 1065663-52-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 274.12 g/mol
Formula C₁₈H₁₅BO₂
badge Registry Numbers
MDL Number MFCD30291691
inventory_2 Storage & Handling
Storage Room temperature, seal, inert gas

description Product Description

Used as a key building block in Suzuki-Miyaura cross-coupling reactions, enabling the synthesis of complex aromatic compounds for applications in organic electronics, pharmaceuticals, and advanced materials. Its boronic acid functionality allows for efficient carbon-carbon bond formation under mild conditions, making it valuable in drug discovery and the development of conjugated polymers for OLEDs and semiconductors. Commonly employed in research settings to construct biaryl and teraryl structures with high selectivity and yield.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿5,500.00
inventory 250mg
10-20 days ฿9,330.00
inventory 1g
10-20 days ฿24,220.00
inventory 5g
10-20 days ฿84,720.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
[1,1':3',1''-Terphenyl]-2'-ylboronic acid
No image available

Used as a key building block in Suzuki-Miyaura cross-coupling reactions, enabling the synthesis of complex aromatic compounds for applications in organic electronics, pharmaceuticals, and advanced materials. Its boronic acid functionality allows for efficient carbon-carbon bond formation under mild conditions, making it valuable in drug discovery and the development of conjugated polymers for OLEDs and semiconductors. Commonly employed in research settings to construct biaryl and teraryl structures with

Used as a key building block in Suzuki-Miyaura cross-coupling reactions, enabling the synthesis of complex aromatic compounds for applications in organic electronics, pharmaceuticals, and advanced materials. Its boronic acid functionality allows for efficient carbon-carbon bond formation under mild conditions, making it valuable in drug discovery and the development of conjugated polymers for OLEDs and semiconductors. Commonly employed in research settings to construct biaryl and teraryl structures with high selectivity and yield.

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...