(S)-(-)-4-PYRROLIDINOPYRINDINYL(PENTAMETHYLCYCLOPENTADIENYL)IRON

≥95%

Reagent Code: #236281
fingerprint
CAS Number 217459-11-5

science Other reagents with same CAS 217459-11-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 376.32 g/mol
Formula C₂₂H₂₈FeN₂
badge Registry Numbers
MDL Number MFCD03427333
inventory_2 Storage & Handling
Storage Room temperature, seal, dry

description Product Description

Used as a chiral organometallic catalyst in asymmetric synthesis, enabling enantioselective transformations in pharmaceutical and fine chemical manufacturing. Its iron-based structure with a pentamethylcyclopentadienyl ligand provides high reactivity and stability under various reaction conditions. Particularly effective in stereoselective C–H activation and cross-coupling reactions, allowing efficient construction of complex organic molecules with defined stereochemistry. Also employed in academic research to develop new catalytic methodologies for sustainable and atom-economical processes.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿12,210.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
(S)-(-)-4-PYRROLIDINOPYRINDINYL(PENTAMETHYLCYCLOPENTADIENYL)IRON
No image available

Used as a chiral organometallic catalyst in asymmetric synthesis, enabling enantioselective transformations in pharmaceutical and fine chemical manufacturing. Its iron-based structure with a pentamethylcyclopentadienyl ligand provides high reactivity and stability under various reaction conditions. Particularly effective in stereoselective C–H activation and cross-coupling reactions, allowing efficient construction of complex organic molecules with defined stereochemistry. Also employed in academic resea

Used as a chiral organometallic catalyst in asymmetric synthesis, enabling enantioselective transformations in pharmaceutical and fine chemical manufacturing. Its iron-based structure with a pentamethylcyclopentadienyl ligand provides high reactivity and stability under various reaction conditions. Particularly effective in stereoselective C–H activation and cross-coupling reactions, allowing efficient construction of complex organic molecules with defined stereochemistry. Also employed in academic research to develop new catalytic methodologies for sustainable and atom-economical processes.

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...