(R)-(-)-BNP acid
98%
- Product Code: 113884
Alias:
(R)-(-)-Binaphthol Phosphate ; R-Binaphthol Phosphate
CAS:
39648-67-4
| 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:
(R)-(-)-BNP acid is primarily utilized in the field of organic synthesis and pharmaceutical research. It serves as a chiral building block for the preparation of various bioactive compounds, particularly in the development of enantioselective drugs. Its application is significant in the synthesis of complex molecules where stereochemistry plays a crucial role in biological activity. Additionally, it is employed in the study of enzyme mechanisms and receptor interactions, aiding in the design of more effective and selective therapeutic agents. The compound’s chiral nature makes it valuable in asymmetric synthesis, contributing to the production of optically pure substances.
Product Specification:
| Test | Specification |
|---|---|
| Appearance | White Powder Or Crystals |
| Purity (HPLC) | 97.5-100 |
| Solubility In Methanol | Almost Transparency |
| Infrared Spectrum | Conforms To Structure |
| Specific Rotation | -610 -590 |
| Specific Rotation | -610 -590 |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | $14.55 |
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| 5.000 | 10-20 days | $31.46 |
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| 25.000 | 10-20 days | $110.11 |
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| 100.000 | 10-20 days | $372.42 |
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(R)-(-)-BNP acid
(R)-(-)-BNP acid is primarily utilized in the field of organic synthesis and pharmaceutical research. It serves as a chiral building block for the preparation of various bioactive compounds, particularly in the development of enantioselective drugs. Its application is significant in the synthesis of complex molecules where stereochemistry plays a crucial role in biological activity. Additionally, it is employed in the study of enzyme mechanisms and receptor interactions, aiding in the design of more effective and selective therapeutic agents. The compound’s chiral nature makes it valuable in asymmetric synthesis, contributing to the production of optically pure substances.
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