rac-2-(Di-tert-butylphosphino)-1,1'-binaphthyl
98%
- Product Code: 68820
CAS:
255836-67-0
Molecular Weight: | 398.52 g./mol | Molecular Formula: | C₂₈H₃₁P |
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EC Number: | MDL Number: | MFCD03094576 | |
Melting Point: | 148-151 °C | Boiling Point: | |
Density: | Storage Condition: | room temperature |
Product Description:
This chemical is widely used as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions. It plays a crucial role in enabling the synthesis of enantiomerically pure compounds, which are essential in the pharmaceutical industry for producing drugs with high stereoselectivity. Its application extends to hydrogenation, cross-coupling, and other carbon-carbon bond-forming reactions, where it enhances the efficiency and selectivity of the catalytic process. Additionally, it is employed in the development of advanced materials and fine chemicals, contributing to innovations in organic synthesis and industrial chemistry.
Product Specification:
Test | Specification |
---|---|
Melting point | 148 151? |
PURITYHPLC | 98 100% |
APPEARANCE | white to beige powder |
INFRARED SPECTRUM | Conforms to Structure |
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.100 | 10-20 days | ฿2,980.00 |
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0.500 | 10-20 days | ฿8,980.00 |
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1.000 | 10-20 days | ฿16,020.00 |
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rac-2-(Di-tert-butylphosphino)-1,1'-binaphthyl
This chemical is widely used as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions. It plays a crucial role in enabling the synthesis of enantiomerically pure compounds, which are essential in the pharmaceutical industry for producing drugs with high stereoselectivity. Its application extends to hydrogenation, cross-coupling, and other carbon-carbon bond-forming reactions, where it enhances the efficiency and selectivity of the catalytic process. Additionally, it is employed in the development of advanced materials and fine chemicals, contributing to innovations in organic synthesis and industrial chemistry.
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