Dipotassium (R)-1,1'-Binaphthyl-2,2'-disulfonate
98%
- Product Code: 78462
CAS:
1092934-19-4
| Molecular Weight: | 490.63 g./mol | Molecular Formula: | C₂₀H₁₂K₂O₆S₂ |
|---|---|---|---|
| EC Number: | MDL Number: | ||
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature |
Product Description:
Used as a chiral resolving agent in organic synthesis to separate enantiomers of racemic compounds. Applied in asymmetric catalysis to induce chirality in reactions, enhancing the production of optically active molecules. Utilized in the development of chiral stationary phases for chromatographic separation of enantiomers. Plays a role in the synthesis of pharmaceuticals, agrochemicals, and fine chemicals where stereoselectivity is critical. Also employed in research for studying chiral recognition and molecular interactions.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | White - Almost white Crystal - Powder |
| PURITY | 97.5-100 |
| Specific rotation 20Dc1 MeOH | 60.0-+65.0 |
| Infrared spectrum | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.010 | 10-20 days | ฿4,250.00 |
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Dipotassium (R)-1,1'-Binaphthyl-2,2'-disulfonate
Used as a chiral resolving agent in organic synthesis to separate enantiomers of racemic compounds. Applied in asymmetric catalysis to induce chirality in reactions, enhancing the production of optically active molecules. Utilized in the development of chiral stationary phases for chromatographic separation of enantiomers. Plays a role in the synthesis of pharmaceuticals, agrochemicals, and fine chemicals where stereoselectivity is critical. Also employed in research for studying chiral recognition and molecular interactions.
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