(E)-3-(3-boronophenyl)acrylic acid

95%

Reagent Code: #184834
fingerprint
CAS Number 843662-48-6

science Other reagents with same CAS 843662-48-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 191.979 g/mol
Formula C₉H₉BO₄
inventory_2 Storage & Handling
Storage 2-8°C, Inert Gas

description Product Description

Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions for the synthesis of complex organic molecules, particularly in pharmaceuticals and agrochemicals. Its boronic acid functionality enables efficient carbon-carbon bond formation under mild conditions. Commonly employed in the preparation of biaryl compounds and conjugated systems found in functional materials and bioactive compounds. Also utilized in research for developing novel anti-inflammatory and anticancer agents due to its structural similarity to cinnamic acid derivatives.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿2,560.00
inventory 250mg
10-20 days ฿3,610.00
inventory 1g
10-20 days ฿8,030.00
inventory 5g
10-20 days ฿32,400.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
(E)-3-(3-boronophenyl)acrylic acid
No image available

Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions for the synthesis of complex organic molecules, particularly in pharmaceuticals and agrochemicals. Its boronic acid functionality enables efficient carbon-carbon bond formation under mild conditions. Commonly employed in the preparation of biaryl compounds and conjugated systems found in functional materials and bioactive compounds. Also utilized in research for developing novel anti-inflammatory and anticancer agents due to its struct

Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions for the synthesis of complex organic molecules, particularly in pharmaceuticals and agrochemicals. Its boronic acid functionality enables efficient carbon-carbon bond formation under mild conditions. Commonly employed in the preparation of biaryl compounds and conjugated systems found in functional materials and bioactive compounds. Also utilized in research for developing novel anti-inflammatory and anticancer agents due to its structural similarity to cinnamic acid derivatives.

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...