1,1'-Binaphthyl-2,2'-diyl hydrogenphosphate
99%
Reagent
Code: #127136
Alias
(±)-2,2'-Dihydroxy-1,1'-binaphthyl hydrogen phosphate; racemic binaphthol phosphate
CAS Number
35193-63-6
blur_circular Chemical Specifications
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Molecular Information
Weight
348.29 g/mol
Formula
C₂₀H₁₃O₄P
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Registry Numbers
EC Number
252-425-8
MDL Number
MFCD00010045
thermostat
Physical Properties
Melting Point
≥300 °C
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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 |
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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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