(1S)-2′-[[Bis(1-methylethyl)amino]carbonyl][1,1′-binaphthalene]-2-carboxylicacid
- Product Code: 237675
CAS:
2646621-99-8
| Molecular Weight: | 425.52 g./mol | Molecular Formula: | C₂₈H₂₇NO₃ |
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| Density: | Storage Condition: | Room temperature, seal, dry |
Product Description:
Widely used as a chiral derivatizing agent in asymmetric synthesis, this compound plays a key role in the preparation of chiral ligands and catalysts. Its rigid binaphthyl backbone provides excellent stereocontrol, making it valuable in enantioselective transformations such as C–C bond-forming reactions and kinetic resolutions. It is particularly effective in the development of organocatalysts and in coordination with metals for use in asymmetric catalysis. Due to its bulky bis(1-methylethyl)amino carbonyl group, it enhances selectivity and stability in catalytic systems. Commonly employed in pharmaceutical and fine chemical industries for synthesizing enantiomerically pure compounds.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 100mg | 10-20 days | ฿25,750.00 |
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(1S)-2′-[[Bis(1-methylethyl)amino]carbonyl][1,1′-binaphthalene]-2-carboxylicacid
Widely used as a chiral derivatizing agent in asymmetric synthesis, this compound plays a key role in the preparation of chiral ligands and catalysts. Its rigid binaphthyl backbone provides excellent stereocontrol, making it valuable in enantioselective transformations such as C–C bond-forming reactions and kinetic resolutions. It is particularly effective in the development of organocatalysts and in coordination with metals for use in asymmetric catalysis. Due to its bulky bis(1-methylethyl)amino carbonyl group, it enhances selectivity and stability in catalytic systems. Commonly employed in pharmaceutical and fine chemical industries for synthesizing enantiomerically pure compounds.
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