(R)-()-5,5',6,6',7,7',8,8'-Octahydro-1,1'-bi-2-naphthol

98%

Reagent Code: #230026
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CAS Number 65355-14-8

science Other reagents with same CAS 65355-14-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 294.39 g/mol
Formula C₂₀H₂₂O₂
badge Registry Numbers
MDL Number MFCD02093485
thermostat Physical Properties
Melting Point 160-166°C (Lit.)
inventory_2 Storage & Handling
Storage Room temperature, seal, dry

description Product Description

Used as a chiral ligand in asymmetric synthesis, particularly in catalytic reactions such as asymmetric hydrogenation and enantioselective C–C bond formation. Its rigid binaphthyl backbone provides excellent stereocontrol, making it valuable in the preparation of optically active pharmaceuticals and fine chemicals. Commonly employed in transition metal complexes with ruthenium, rhodium, or titanium to achieve high enantioselectivity. Also applied in chiral resolution and as a building block for chiral sensors and materials.

Available Sizes & Pricing

Size Availability Unit Price Quantity
1g
10-20 days ฿380.00
5g
10-20 days ฿1,350.00
25g
10-20 days ฿5,800.00
100g
10-20 days ฿23,090.00
(R)-()-5,5',6,6',7,7',8,8'-Octahydro-1,1'-bi-2-naphthol
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Used as a chiral ligand in asymmetric synthesis, particularly in catalytic reactions such as asymmetric hydrogenation and enantioselective C–C bond formation. Its rigid binaphthyl backbone provides excellent stereocontrol, making it valuable in the preparation of optically active pharmaceuticals and fine chemicals. Commonly employed in transition metal complexes with ruthenium, rhodium, or titanium to achieve high enantioselectivity. Also applied in chiral resolution and as a building block for chiral se

Used as a chiral ligand in asymmetric synthesis, particularly in catalytic reactions such as asymmetric hydrogenation and enantioselective C–C bond formation. Its rigid binaphthyl backbone provides excellent stereocontrol, making it valuable in the preparation of optically active pharmaceuticals and fine chemicals. Commonly employed in transition metal complexes with ruthenium, rhodium, or titanium to achieve high enantioselectivity. Also applied in chiral resolution and as a building block for chiral sensors and materials.

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