2-(3-bromophenyl)-5,5-dimethyl-1,3,2-dioxaborinane

98%

Reagent Code: #148010
fingerprint
CAS Number 635305-38-3

science Other reagents with same CAS 635305-38-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 268.943 g/mol
Formula C₁₁H₁₄BBrO₂
inventory_2 Storage & Handling
Storage 2-8℃

description Product Description

Used as a boronic ester reagent in Suzuki-Miyaura cross-coupling reactions to form carbon-carbon bonds in organic synthesis. It serves as a stable and selective boron-containing partner for palladium-catalyzed coupling with aryl or vinyl halides, enabling the construction of biaryl frameworks common in pharmaceuticals and functional materials. The 3-bromophenyl group allows for further functionalization, while the dimethyl dioxaborinane ring enhances stability and reactivity profile compared to simple boronic acids.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿660.00
inventory 1g
10-20 days ฿1,660.00
inventory 5g
10-20 days ฿6,000.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
2-(3-bromophenyl)-5,5-dimethyl-1,3,2-dioxaborinane
No image available

Used as a boronic ester reagent in Suzuki-Miyaura cross-coupling reactions to form carbon-carbon bonds in organic synthesis. It serves as a stable and selective boron-containing partner for palladium-catalyzed coupling with aryl or vinyl halides, enabling the construction of biaryl frameworks common in pharmaceuticals and functional materials. The 3-bromophenyl group allows for further functionalization, while the dimethyl dioxaborinane ring enhances stability and reactivity profile compared to simple bo

Used as a boronic ester reagent in Suzuki-Miyaura cross-coupling reactions to form carbon-carbon bonds in organic synthesis. It serves as a stable and selective boron-containing partner for palladium-catalyzed coupling with aryl or vinyl halides, enabling the construction of biaryl frameworks common in pharmaceuticals and functional materials. The 3-bromophenyl group allows for further functionalization, while the dimethyl dioxaborinane ring enhances stability and reactivity profile compared to simple boronic acids.

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...