1-Cyclooctyl-3-mesityl-1H-imidazol-3-ium chloride

97%

Reagent Code: #164157
fingerprint
CAS Number 1583244-05-6

science Other reagents with same CAS 1583244-05-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 332.91 g/mol
Formula C₂₀H₂₉ClN₂
badge Registry Numbers
MDL Number MFCD34563814
inventory_2 Storage & Handling
Storage Room temperature, dry, light-proof

description Product Description

Used as a precursor for N-heterocyclic carbene (NHC) ligands in organometallic catalysis. Its bulky cyclooctyl and mesityl groups enhance steric protection around metal centers, improving catalyst stability and selectivity. Commonly applied in cross-coupling reactions, olefin metathesis, and hydrogenation processes. The chloride counterion facilitates easy substitution for various metal complexes. Effective in both academic research and industrial catalytic systems due to its tunable electronic and steric properties.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿3,290.00
inventory 250mg
10-20 days ฿5,440.00
inventory 1g
10-20 days ฿17,560.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
1-Cyclooctyl-3-mesityl-1H-imidazol-3-ium chloride
No image available

Used as a precursor for N-heterocyclic carbene (NHC) ligands in organometallic catalysis. Its bulky cyclooctyl and mesityl groups enhance steric protection around metal centers, improving catalyst stability and selectivity. Commonly applied in cross-coupling reactions, olefin metathesis, and hydrogenation processes. The chloride counterion facilitates easy substitution for various metal complexes. Effective in both academic research and industrial catalytic systems due to its tunable electronic and steri

Used as a precursor for N-heterocyclic carbene (NHC) ligands in organometallic catalysis. Its bulky cyclooctyl and mesityl groups enhance steric protection around metal centers, improving catalyst stability and selectivity. Commonly applied in cross-coupling reactions, olefin metathesis, and hydrogenation processes. The chloride counterion facilitates easy substitution for various metal complexes. Effective in both academic research and industrial catalytic systems due to its tunable electronic and steric properties.

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...