(S)-4-[2-(Diphenylphosphino)-1-naphthalenyl]-N-[(R)-1-phenylethyl]-1-phthalazinamine

98%

Reagent Code: #38507
fingerprint
CAS Number 828927-96-4

science Other reagents with same CAS 828927-96-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 559.6400 g/mol
Formula C₃₈H₃₀N₃P
badge Registry Numbers
MDL Number MFCD09264274
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

This chemical is primarily utilized as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions. It plays a significant role in facilitating enantioselective transformations, such as hydrogenation, allylic alkylation, and cross-coupling reactions. Its unique structure, featuring both a diphenylphosphino group and a phthalazine moiety, allows for effective coordination with metal centers, enhancing stereocontrol in the synthesis of chiral molecules. This makes it valuable in the production of pharmaceuticals, agrochemicals, and fine chemicals where high enantiomeric purity is crucial. Additionally, its application extends to the development of novel catalytic systems for organic synthesis, contributing to advancements in green and sustainable chemistry practices.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿5,000.00
inventory 250mg
10-20 days ฿11,960.00
inventory 1g
10-20 days ฿47,680.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
(S)-4-[2-(Diphenylphosphino)-1-naphthalenyl]-N-[(R)-1-phenylethyl]-1-phthalazinamine
No image available

This chemical is primarily utilized as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions. It plays a significant role in facilitating enantioselective transformations, such as hydrogenation, allylic alkylation, and cross-coupling reactions. Its unique structure, featuring both a diphenylphosphino group and a phthalazine moiety, allows for effective coordination with metal centers, enhancing stereocontrol in the synthesis of chiral molecules. This makes it valua

This chemical is primarily utilized as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions. It plays a significant role in facilitating enantioselective transformations, such as hydrogenation, allylic alkylation, and cross-coupling reactions. Its unique structure, featuring both a diphenylphosphino group and a phthalazine moiety, allows for effective coordination with metal centers, enhancing stereocontrol in the synthesis of chiral molecules. This makes it valuable in the production of pharmaceuticals, agrochemicals, and fine chemicals where high enantiomeric purity is crucial. Additionally, its application extends to the development of novel catalytic systems for organic synthesis, contributing to advancements in green and sustainable chemistry practices.

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...