1,1'-Binaphthyl-2,2'-diyl hydrogenphosphate

99%

Reagent Code: #127136
label
Alias (±)-2,2'-Dihydroxy-1,1'-binaphthyl hydrogen phosphate; racemic binaphthol phosphate
fingerprint
CAS Number 35193-63-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 348.29 g/mol
Formula C₂₀H₁₃O₄P
badge Registry Numbers
EC Number 252-425-8
MDL Number MFCD00010045
thermostat Physical Properties
Melting Point ≥300 °C
inventory_2 Storage & Handling
Storage room temperature

description Product Description

1,1'-Binaphthyl-2,2'-diyl hydrogenphosphate is primarily utilized as a chiral resolving agent in the field of asymmetric synthesis. It is often employed to separate enantiomers of chiral compounds, particularly in the pharmaceutical industry where the purity of a specific enantiomer is crucial for drug efficacy and safety. The compound's ability to form diastereomeric complexes with chiral molecules makes it valuable in chromatographic techniques, such as high-performance liquid chromatography (HPLC), for the resolution of racemic mixtures. Additionally, it serves as a precursor or intermediate in the synthesis of more complex chiral ligands and catalysts used in enantioselective reactions, contributing to the development of optically active compounds in organic chemistry.

format_list_bulleted Product Specification

Test Parameter Specification
Purity (HPLC) 99
Purity (Titration with NaOH) 98.5-101.5
Appearance White To Off-White Powder, Crystals And/Or Chunks
Infrared Spectrum Conforms To Structure
Solubility in N,N-DMF Almost transparent

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿600.00
inventory 100g
10-20 days ฿11,320.00
inventory 25g
10-20 days ฿4,410.00
inventory 5g
10-20 days ฿1,550.00
1,1'-Binaphthyl-2,2'-diyl hydrogenphosphate
1,1'-Binaphthyl-2,2'-diyl hydrogenphosphate is primarily utilized as a chiral resolving agent in the field of asymmetric synthesis. It is often employed to separate enantiomers of chiral compounds, particularly in the pharmaceutical industry where the purity of a specific enantiomer is crucial for drug efficacy and safety. The compound's ability to form diastereomeric complexes with chiral molecules makes it valuable in chromatographic techniques, such as high-performance liquid chromatography (HPLC), for the resolution of racemic mixtures. Additionally, it serves as a precursor or intermediate in the synthesis of more complex chiral ligands and catalysts used in enantioselective reactions, contributing to the development of optically active compounds in organic chemistry.
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