(Bathocuproine)NiBr2

≥98%

Reagent Code: #149508
fingerprint
CAS Number 326822-02-0

science Other reagents with same CAS 326822-02-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 578.95 g/mol
Formula C₂₆H₂₀Br₂N₂Ni
badge Registry Numbers
MDL Number MFCD31807323
thermostat Physical Properties
Melting Point >300 °C
inventory_2 Storage & Handling
Storage 2-8°C, inert gas, sealed

description Product Description

Used as a catalyst in cross-coupling reactions, particularly in the formation of carbon-nitrogen and carbon-carbon bonds. It enables efficient amination and etherification processes under mild conditions, making it valuable in pharmaceutical and agrochemical synthesis. Its stability and selectivity enhance yields in reactions involving aryl halides and heteroaromatic compounds. Also applied in materials science for constructing conjugated organic frameworks through catalyzed coupling steps.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿4,290.00
inventory 250mg
10-20 days ฿6,960.00
inventory 1g
10-20 days ฿12,690.00
inventory 5g
10-20 days ฿48,980.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
(Bathocuproine)NiBr2
No image available

Used as a catalyst in cross-coupling reactions, particularly in the formation of carbon-nitrogen and carbon-carbon bonds. It enables efficient amination and etherification processes under mild conditions, making it valuable in pharmaceutical and agrochemical synthesis. Its stability and selectivity enhance yields in reactions involving aryl halides and heteroaromatic compounds. Also applied in materials science for constructing conjugated organic frameworks through catalyzed coupling steps.

Used as a catalyst in cross-coupling reactions, particularly in the formation of carbon-nitrogen and carbon-carbon bonds. It enables efficient amination and etherification processes under mild conditions, making it valuable in pharmaceutical and agrochemical synthesis. Its stability and selectivity enhance yields in reactions involving aryl halides and heteroaromatic compounds. Also applied in materials science for constructing conjugated organic frameworks through catalyzed coupling steps.

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...