1,8-Bis(diphenylphosphino)naphthalene

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Reagent Code: #68737
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CAS Number 153725-04-3

science Other reagents with same CAS 153725-04-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 496.53 g/mol
Formula C₃₄H₂₆P₂
inventory_2 Storage & Handling
Storage room temperature, dry

description Product Description

1,8-Bis(diphenylphosphino)naphthalene is widely used as a ligand in coordination chemistry and catalysis. Its unique structure allows it to stabilize transition metal complexes, making it valuable in various catalytic processes, including hydrogenation, cross-coupling reactions, and carbonylation. The compound's ability to form stable complexes with metals like palladium, platinum, and rhodium enhances the efficiency and selectivity of these reactions. Additionally, it is employed in the synthesis of organometallic compounds and as a key component in the development of new catalytic systems for industrial and academic research. Its application in asymmetric catalysis is particularly notable, where it helps in producing chiral molecules with high enantioselectivity.

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Test Parameter Specification
Appearance Light orange to yellow to green powder to crystal
Purity 96.5-100
Infrared Spectrum Conforms to Structure

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Size Availability Unit Price Quantity
inventory 200mg
10-20 days ฿2,880.00
inventory 1g
10-20 days ฿9,050.00

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1,8-Bis(diphenylphosphino)naphthalene
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1,8-Bis(diphenylphosphino)naphthalene is widely used as a ligand in coordination chemistry and catalysis. Its unique structure allows it to stabilize transition metal complexes, making it valuable in various catalytic processes, including hydrogenation, cross-coupling reactions, and carbonylation. The compound's ability to form stable complexes with metals like palladium, platinum, and rhodium enhances the efficiency and selectivity of these reactions. Additionally, it is employed in the synthesis of org

1,8-Bis(diphenylphosphino)naphthalene is widely used as a ligand in coordination chemistry and catalysis. Its unique structure allows it to stabilize transition metal complexes, making it valuable in various catalytic processes, including hydrogenation, cross-coupling reactions, and carbonylation. The compound's ability to form stable complexes with metals like palladium, platinum, and rhodium enhances the efficiency and selectivity of these reactions. Additionally, it is employed in the synthesis of organometallic compounds and as a key component in the development of new catalytic systems for industrial and academic research. Its application in asymmetric catalysis is particularly notable, where it helps in producing chiral molecules with high enantioselectivity.

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