S-()-1,1'-Binaphthyl-2,2'-diyl hydrogen phosphate

97%

  • Product Code: 121742
  Alias:    (S)-(+)-Binaphthol Phosphate ; (S)-Binaphthol Phosphate
  CAS:    35193-64-7
Molecular Weight: 348.29 g./mol Molecular Formula: C₂₀H₁₃O₄P
EC Number: MDL Number: MFCD00010045
Melting Point: ≥300 °C Boiling Point:
Density: Storage Condition: 2~8°C
Product Description: S-()-1,1'-Binaphthyl-2,2'-diyl hydrogen phosphate is widely used as a chiral resolving agent in the separation of enantiomers, particularly in pharmaceutical and chemical research. It is effective in forming diastereomeric salts with racemic mixtures, enabling the purification of optically active compounds. This chemical is also employed in asymmetric synthesis as a chiral catalyst or ligand, facilitating the production of enantiomerically pure substances. Additionally, it finds application in the development of chiral stationary phases for high-performance liquid chromatography (HPLC), enhancing the separation efficiency of chiral molecules. Its role in these processes is crucial for advancing drug development and ensuring the production of high-purity chiral compounds.
Product Specification:
Test Specification
Purity (HPLC) 97-100
Specific Rotation 580 Degree Celsius - 610 Degree Celsius
Specific Rotation 580 610°
Appearance White Solid Or Powder
Infrared Spectrum Conforms To Structure
Solubility In Pyridine Colorless To Faint Yellow, Clear To Slightly Hazy 5%
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
1.000 10-20 days ฿390.00
+
-
5.000 10-20 days ฿1,350.00
+
-
25.000 10-20 days ฿4,670.00
+
-
S-()-1,1'-Binaphthyl-2,2'-diyl hydrogen phosphate
S-()-1,1'-Binaphthyl-2,2'-diyl hydrogen phosphate is widely used as a chiral resolving agent in the separation of enantiomers, particularly in pharmaceutical and chemical research. It is effective in forming diastereomeric salts with racemic mixtures, enabling the purification of optically active compounds. This chemical is also employed in asymmetric synthesis as a chiral catalyst or ligand, facilitating the production of enantiomerically pure substances. Additionally, it finds application in the development of chiral stationary phases for high-performance liquid chromatography (HPLC), enhancing the separation efficiency of chiral molecules. Its role in these processes is crucial for advancing drug development and ensuring the production of high-purity chiral compounds.
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