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

98%

Reagent Code: #70368
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CAS Number 828927-97-5

science Other reagents with same CAS 828927-97-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 559.64 g/mol
Formula C₃₈H₃₀N₃P
badge Registry Numbers
MDL Number MFCD09264274
inventory_2 Storage & Handling
Storage 2-8°C, protected from light, stored under inert gas

description Product Description

This chemical is primarily utilized as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions. Its structure, featuring a diphenylphosphino group and a chiral phenylethylamine moiety, makes it highly effective in inducing enantioselectivity. It is commonly employed in asymmetric hydrogenation, a process crucial for producing enantiomerically pure compounds in pharmaceuticals and fine chemicals. Additionally, it finds use in C-C bond-forming reactions, such as asymmetric allylic alkylation, where it helps achieve high stereocontrol. Its application extends to the synthesis of complex organic molecules, where precise chiral induction is essential.

Available Sizes & Pricing

Size Availability Unit Price Quantity
1g
10-20 days ฿39,312.00
250mg
10-20 days ฿12,294.00
100mg
10-20 days ฿6,228.00
(R)-4-[2-(Diphenylphosphino)-1-naphthalenyl]-N-[(R)-1-phenylethyl]-1-phthalazinamine
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This chemical is primarily utilized as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions. Its structure, featuring a diphenylphosphino group and a chiral phenylethylamine moiety, makes it highly effective in inducing enantioselectivity. It is commonly employed in asymmetric hydrogenation, a process crucial for producing enantiomerically pure compounds in pharmaceuticals and fine chemicals. Additionally, it finds use in C-C bond-forming reactions, such as asymme

This chemical is primarily utilized as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions. Its structure, featuring a diphenylphosphino group and a chiral phenylethylamine moiety, makes it highly effective in inducing enantioselectivity. It is commonly employed in asymmetric hydrogenation, a process crucial for producing enantiomerically pure compounds in pharmaceuticals and fine chemicals. Additionally, it finds use in C-C bond-forming reactions, such as asymmetric allylic alkylation, where it helps achieve high stereocontrol. Its application extends to the synthesis of complex organic molecules, where precise chiral induction is essential.

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