1,1'-Binaphthyl-2,2'-diyl hydrogenphosphate
99%
- Product Code: 127136
Alias:
(±)-2,2'-Dihydroxy-1,1'-binaphthyl hydrogen phosphate; racemic binaphthol phosphate
CAS:
35193-63-6
| Molecular Weight: | 348.29 g./mol | Molecular Formula: | C₂₀H₁₃O₄P |
|---|---|---|---|
| EC Number: | 252-425-8 | MDL Number: | MFCD00010045 |
| Melting Point: | ≥300 °C | Boiling Point: | |
| Density: | Storage Condition: | room temperature |
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.
Product Specification:
| Test | 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 Transparency |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿600.00 |
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| 5.000 | 10-20 days | ฿1,550.00 |
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| 25.000 | 10-20 days | ฿4,410.00 |
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| 100.000 | 10-20 days | ฿11,320.00 |
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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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