(S,S)-1,2-Bis(t-butylmethylphosphino)benzene (S,S)-BenzP

98%

Reagent Code: #38652
fingerprint
CAS Number 1355162-85-4

science Other reagents with same CAS 1355162-85-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 282.3400 g/mol
Formula C₁₆H₂₈P₂
badge Registry Numbers
MDL Number MFCD18837015
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

(S,S)-BenzP is primarily used as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions. It is highly effective in enantioselective hydrogenation, where it helps produce chiral molecules with high selectivity. This makes it valuable in the synthesis of pharmaceuticals, agrochemicals, and fine chemicals, where precise stereochemistry is crucial. Its robust structure and ability to form stable complexes with metals like rhodium and iridium enhance its utility in creating complex organic compounds with high enantiomeric purity.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿5,220.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
(S,S)-1,2-Bis(t-butylmethylphosphino)benzene (S,S)-BenzP
No image available

(S,S)-BenzP is primarily used as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions. It is highly effective in enantioselective hydrogenation, where it helps produce chiral molecules with high selectivity. This makes it valuable in the synthesis of pharmaceuticals, agrochemicals, and fine chemicals, where precise stereochemistry is crucial. Its robust structure and ability to form stable complexes with metals like rhodium and iridium enhance its utility in creat

(S,S)-BenzP is primarily used as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions. It is highly effective in enantioselective hydrogenation, where it helps produce chiral molecules with high selectivity. This makes it valuable in the synthesis of pharmaceuticals, agrochemicals, and fine chemicals, where precise stereochemistry is crucial. Its robust structure and ability to form stable complexes with metals like rhodium and iridium enhance its utility in creating complex organic compounds with high enantiomeric purity.

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...